Canonical Allele Identifier: CA1603608845

Linked Data

dbSNP Id: rs1763220513

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177404138_177404145dup , CM000667.2:g.177404138_177404145dup GRCh38
NC_000005.9:g.176831139_176831146dup , CM000667.1:g.176831139_176831146dup GRCh37
NC_000005.8:g.176763745_176763752dup NCBI36
NG_007568.1:g.10432_10439dup , LRG_145:g.10432_10439dup

Transcript Alleles

HGVS Amino-acid change
ENST00000696192.1:c.*684+51_*685-48dup (F12) ENSP00000512476.1:n.*684+51_*685-48dup
ENST00000696193.1:c.*1389-38_*1389-31dup (F12) ENSP00000512477.1:n.*1389-38_*1389-31dup
ENST00000696194.1:c.*608+51_*609-48dup (F12) ENSP00000512478.1:n.*608+51_*609-48dup
ENST00000696195.1:n.3821+51_3822-48dup (F12)
ENST00000696200.1:n.1121+51_1122-48dup (F12)
ENST00000696201.1:c.1018+51_1019-48dup (F12) ENSP00000512482.1:n.1018+51_1019-48dup
ENST00000253496.4:c.1018+51_1019-48dup (F12) MANE Select ENSP00000253496.3:n.1018+51_1019-48dup
ENST00000253496.3:c.1018+51_1019-48dup (F12) ENSP00000253496.3:n.1018+51_1019-48dup
ENST00000502598.5:c.-45+612_-45+619dup (GRK6) ENSP00000422873.1:n.-45+612_-45+619dup
ENST00000502854.5:n.277+51_278-48dup (F12)
ENST00000503736.1:n.390+51_391-48dup (F12)
ENST00000510358.5:n.328_335dup (F12)
NM_000505.3:c.1018+51_1019-48dup , LRG_145t1:c.1018+51_1019-48dup (F12) NP_000496.2:n.1018+51_1019-48dup
XM_011534461.1:c.1018+51_1019-48dup (F12) XP_011532763.1:n.1018+51_1019-48dup
XM_011534462.1:c.682+51_683-48dup (F12) XP_011532764.1:n.682+51_683-48dup
XM_011534462.2:c.682+51_683-48dup (F12) XP_011532764.1:n.682+51_683-48dup
XM_017009773.2:c.1416+7064_1416+7071dup (SLC34A1) XP_016865262.1:n.1416+7064_1416+7071dup
NM_000505.4:c.1018+51_1019-48dup (F12) MANE Select NP_000496.2:n.1018+51_1019-48dup