Canonical Allele Identifier: CA367870572
Gene: ELN HGNC NCBI

Linked Data

gnomAD v4: 7-74048201-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74048201G>T , CM000669.2:g.74048201G>T GRCh38
NC_000007.13:g.73462531G>T , CM000669.1:g.73462531G>T GRCh37
NC_000007.12:g.73100467G>T NCBI36
NG_009261.1:g.25105G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000692049.1:c.745G>T ENSP00000510104.1:p.Gly249Trp
ENST00000252034.12:c.745G>T MANE Select ENSP00000252034.7:p.Gly249Trp
ENST00000252034.11:c.745G>T ENSP00000252034.7:p.Gly249Trp
ENST00000320399.10:c.745G>T ENSP00000313565.6:p.Gly249Trp
ENST00000320492.11:c.637G>T ENSP00000315607.7:p.Gly213Trp
ENST00000357036.9:c.760G>T ENSP00000349540.5:p.Gly254Trp
ENST00000358929.8:c.745G>T ENSP00000351807.5:p.Gly249Trp
ENST00000380553.8:c.394G>T ENSP00000369926.4:p.Gly132Trp
ENST00000380562.8:c.745G>T ENSP00000369936.4:p.Gly249Trp
ENST00000380575.8:c.715G>T ENSP00000369949.4:p.Gly239Trp
ENST00000380576.9:c.745G>T ENSP00000369950.5:p.Gly249Trp
ENST00000380584.8:c.703G>T ENSP00000369958.4:p.Gly235Trp
ENST00000414324.5:c.730G>T ENSP00000392575.1:p.Gly244Trp
ENST00000417091.5:c.643G>T
ENST00000428787.5:c.499G>T
ENST00000429192.5:c.760G>T ENSP00000391129.1:p.Gly254Trp
ENST00000438880.5:c.328G>T ENSP00000389206.1:p.Gly110Trp
ENST00000438906.5:c.679G>T ENSP00000406949.1:p.Gly227Trp
ENST00000445912.5:c.745G>T ENSP00000389857.1:p.Gly249Trp
ENST00000458204.5:c.715G>T ENSP00000403162.1:p.Gly239Trp
ENST00000493839.1:n.211G>T
ENST00000621115.4:c.613G>T ENSP00000480955.1:p.Gly205Trp
NM_000501.3:c.745G>T NP_000492.2:p.Gly249Trp
NM_001081752.2:c.715G>T NP_001075221.1:p.Gly239Trp
NM_001081753.2:c.760G>T NP_001075222.1:p.Gly254Trp
NM_001081754.2:c.760G>T NP_001075223.1:p.Gly254Trp
NM_001081755.2:c.745G>T NP_001075224.1:p.Gly249Trp
NM_001278912.1:c.745G>T NP_001265841.1:p.Gly249Trp
NM_001278913.1:c.637G>T NP_001265842.1:p.Gly213Trp
NM_001278914.1:c.730G>T NP_001265843.1:p.Gly244Trp
NM_001278915.1:c.745G>T NP_001265844.1:p.Gly249Trp
NM_001278916.1:c.703G>T NP_001265845.1:p.Gly235Trp
NM_001278917.1:c.715G>T NP_001265846.1:p.Gly239Trp
NM_001278918.1:c.613G>T NP_001265847.1:p.Gly205Trp
NM_001278939.1:c.745G>T NP_001265868.1:p.Gly249Trp
XM_005250187.1:c.709G>T XP_005250244.1:p.Gly237Trp
XM_005250188.1:c.703G>T XP_005250245.1:p.Gly235Trp
XM_011515868.1:c.760G>T XP_011514170.1:p.Gly254Trp
XM_011515869.1:c.730G>T XP_011514171.1:p.Gly244Trp
XM_011515870.1:c.724G>T XP_011514172.1:p.Gly242Trp
XM_011515871.1:c.718G>T XP_011514173.1:p.Gly240Trp
XM_011515872.1:c.760G>T XP_011514174.1:p.Gly254Trp
XM_011515873.1:c.760G>T XP_011514175.1:p.Gly254Trp
XM_011515874.1:c.694G>T XP_011514176.1:p.Gly232Trp
XM_011515875.1:c.679G>T XP_011514177.1:p.Gly227Trp
XM_011515876.1:c.760G>T XP_011514178.1:p.Gly254Trp
XM_011515877.1:c.760G>T XP_011514179.1:p.Gly254Trp
XM_005250187.2:c.709G>T XP_005250244.1:p.Gly237Trp
XM_005250188.2:c.703G>T XP_005250245.1:p.Gly235Trp
XM_011515868.2:c.760G>T XP_011514170.1:p.Gly254Trp
XM_011515871.2:c.718G>T XP_011514173.1:p.Gly240Trp
XM_011515872.2:c.760G>T XP_011514174.1:p.Gly254Trp
XM_011515873.2:c.760G>T XP_011514175.1:p.Gly254Trp
XM_011515875.2:c.679G>T XP_011514177.1:p.Gly227Trp
XM_011515876.2:c.760G>T XP_011514178.1:p.Gly254Trp
XM_011515877.2:c.760G>T XP_011514179.1:p.Gly254Trp
XM_017011813.1:c.673G>T XP_016867302.1:p.Gly225Trp
XM_017011814.2:c.718G>T XP_016867303.1:p.Gly240Trp
NM_000501.4:c.745G>T MANE Select NP_000492.2:p.Gly249Trp
NM_001081752.3:c.715G>T NP_001075221.1:p.Gly239Trp
NM_001081753.3:c.760G>T NP_001075222.1:p.Gly254Trp
NM_001081754.3:c.760G>T NP_001075223.1:p.Gly254Trp
NM_001081755.3:c.745G>T NP_001075224.1:p.Gly249Trp
NM_001278912.2:c.745G>T NP_001265841.1:p.Gly249Trp
NM_001278913.2:c.637G>T NP_001265842.1:p.Gly213Trp
NM_001278914.2:c.730G>T NP_001265843.1:p.Gly244Trp
NM_001278915.2:c.745G>T NP_001265844.1:p.Gly249Trp
NM_001278916.2:c.703G>T NP_001265845.1:p.Gly235Trp
NM_001278917.2:c.715G>T NP_001265846.1:p.Gly239Trp
NM_001278918.2:c.613G>T NP_001265847.1:p.Gly205Trp
NM_001278939.2:c.745G>T NP_001265868.1:p.Gly249Trp