Canonical Allele Identifier: CA160115112

Gene: ELN

Linked Data

• dbSNP Id: rs8326
• gnomAD v3: 7-74069359-G-T
• gnomAD v4: 7-74069359-G-T
• MyVariant Identifiers: chr7:g.73483689G>T (hg19) ; chr7:g.74069359G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74069359G>T , CM000669.2:g.74069359G>T	GRCh38
NC_000007.13:g.73483689G>T , CM000669.1:g.73483689G>T	GRCh37
NC_000007.12:g.73121625G>T	NCBI36
NG_009261.1:g.46263G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252034.12:c.*659G>T MANE Select	ENSP00000252034.7:n.*659G>T
ENST00000252034.11:c.*659G>T	ENSP00000252034.7:n.*659G>T
ENST00000320492.11:c.*659G>T	ENSP00000315607.7:n.*659G>T
ENST00000357036.9:c.*659G>T	ENSP00000349540.5:n.*659G>T
ENST00000358929.8:c.*659G>T	ENSP00000351807.5:n.*659G>T
ENST00000380553.8:c.*659G>T	ENSP00000369926.4:n.*659G>T
ENST00000380575.8:c.*659G>T	ENSP00000369949.4:n.*659G>T
ENST00000380576.9:c.*659G>T	ENSP00000369950.5:n.*659G>T
ENST00000380584.8:c.*659G>T	ENSP00000369958.4:n.*659G>T
ENST00000414324.5:c.*659G>T	ENSP00000392575.1:n.*659G>T
ENST00000429192.5:c.*659G>T	ENSP00000391129.1:n.*659G>T
ENST00000458204.5:c.*659G>T	ENSP00000403162.1:n.*659G>T
ENST00000621115.4:c.*659G>T	ENSP00000480955.1:n.*659G>T
NM_000501.3:c.*659G>T	NP_000492.2:n.*659G>T
NM_001081752.2:c.*659G>T	NP_001075221.1:n.*659G>T
NM_001081753.2:c.*659G>T	NP_001075222.1:n.*659G>T
NM_001081754.2:c.*659G>T	NP_001075223.1:n.*659G>T
NM_001081755.2:c.*659G>T	NP_001075224.1:n.*659G>T
NM_001278912.1:c.*659G>T	NP_001265841.1:n.*659G>T
NM_001278913.1:c.*659G>T	NP_001265842.1:n.*659G>T
NM_001278914.1:c.*659G>T	NP_001265843.1:n.*659G>T
NM_001278915.1:c.*659G>T	NP_001265844.1:n.*659G>T
NM_001278916.1:c.*659G>T	NP_001265845.1:n.*659G>T
NM_001278917.1:c.*659G>T	NP_001265846.1:n.*659G>T
NM_001278918.1:c.*659G>T	NP_001265847.1:n.*659G>T
NM_001278939.1:c.*659G>T	NP_001265868.1:n.*659G>T
XM_005250187.1:c.*659G>T	XP_005250244.1:n.*659G>T
XM_005250188.1:c.*659G>T	XP_005250245.1:n.*659G>T
XM_011515868.1:c.*659G>T	XP_011514170.1:n.*659G>T
XM_011515869.1:c.*659G>T	XP_011514171.1:n.*659G>T
XM_011515870.1:c.*659G>T	XP_011514172.1:n.*659G>T
XM_011515871.1:c.*659G>T	XP_011514173.1:n.*659G>T
XM_011515872.1:c.*659G>T	XP_011514174.1:n.*659G>T
XM_011515873.1:c.*659G>T	XP_011514175.1:n.*659G>T
XM_011515874.1:c.*659G>T	XP_011514176.1:n.*659G>T
XM_011515875.1:c.*659G>T	XP_011514177.1:n.*659G>T
XM_011515876.1:c.*659G>T	XP_011514178.1:n.*659G>T
XM_011515877.1:c.*659G>T	XP_011514179.1:n.*659G>T
XM_005250187.2:c.*659G>T	XP_005250244.1:n.*659G>T
XM_005250188.2:c.*659G>T	XP_005250245.1:n.*659G>T
XM_011515868.2:c.*659G>T	XP_011514170.1:n.*659G>T
XM_011515871.2:c.*659G>T	XP_011514173.1:n.*659G>T
XM_011515872.2:c.*659G>T	XP_011514174.1:n.*659G>T
XM_011515873.2:c.*659G>T	XP_011514175.1:n.*659G>T
XM_011515875.2:c.*659G>T	XP_011514177.1:n.*659G>T
XM_011515876.2:c.*659G>T	XP_011514178.1:n.*659G>T
XM_011515877.2:c.*659G>T	XP_011514179.1:n.*659G>T
XM_017011813.1:c.*659G>T	XP_016867302.1:n.*659G>T
XM_017011814.2:c.*659G>T	XP_016867303.1:n.*659G>T
NM_000501.4:c.*659G>T MANE Select	NP_000492.2:n.*659G>T
NM_001081752.3:c.*659G>T	NP_001075221.1:n.*659G>T
NM_001081753.3:c.*659G>T	NP_001075222.1:n.*659G>T
NM_001081754.3:c.*659G>T	NP_001075223.1:n.*659G>T
NM_001081755.3:c.*659G>T	NP_001075224.1:n.*659G>T
NM_001278912.2:c.*659G>T	NP_001265841.1:n.*659G>T
NM_001278913.2:c.*659G>T	NP_001265842.1:n.*659G>T
NM_001278914.2:c.*659G>T	NP_001265843.1:n.*659G>T
NM_001278915.2:c.*659G>T	NP_001265844.1:n.*659G>T
NM_001278916.2:c.*659G>T	NP_001265845.1:n.*659G>T
NM_001278917.2:c.*659G>T	NP_001265846.1:n.*659G>T
NM_001278918.2:c.*659G>T	NP_001265847.1:n.*659G>T
NM_001278939.2:c.*659G>T	NP_001265868.1:n.*659G>T