Canonical Allele Identifier: CA13202714
Gene: SORCS1 HGNC NCBI

Linked Data

dbSNP Id: rs10884402

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.107033184G>A , CM000672.2:g.107033184G>A GRCh38
NC_000010.10:g.108792942G>A , CM000672.1:g.108792942G>A GRCh37
NC_000010.9:g.108782932G>A NCBI36
NG_029120.1:g.136525C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263054.11:c.559-76604C>T MANE Select ENSP00000263054.5:n.559-76604C>T
ENST00000263054.10:c.559-76604C>T ENSP00000263054.5:n.559-76604C>T
NM_001013031.2:c.559-76604C>T NP_001013049.1:n.559-76604C>T
NM_001206569.1:c.559-76604C>T NP_001193498.1:n.559-76604C>T
NM_001206570.1:c.559-76604C>T NP_001193499.1:n.559-76604C>T
NM_001206571.1:c.559-76604C>T NP_001193500.1:n.559-76604C>T
NM_001206572.1:c.559-76604C>T NP_001193501.1:n.559-76604C>T
NM_052918.4:c.559-76604C>T NP_443150.3:n.559-76604C>T
XM_011539199.1:c.559-76604C>T XP_011537501.1:n.559-76604C>T
XM_011539200.1:c.559-76604C>T XP_011537502.1:n.559-76604C>T
XM_011539201.1:c.559-76604C>T XP_011537503.1:n.559-76604C>T
XM_011539204.1:c.4-76604C>T XP_011537506.1:n.4-76604C>T
XM_011539206.1:c.559-76604C>T XP_011537508.1:n.559-76604C>T
XM_011539199.3:c.559-76604C>T XP_011537501.1:n.559-76604C>T
XM_011539201.3:c.559-76604C>T XP_011537503.1:n.559-76604C>T
XM_017015614.2:c.559-76604C>T XP_016871103.1:n.559-76604C>T
XM_017015615.2:c.559-76604C>T XP_016871104.1:n.559-76604C>T
XM_017015617.1:c.4-76604C>T XP_016871106.1:n.4-76604C>T
NM_001013031.3:c.559-76604C>T NP_001013049.1:n.559-76604C>T
NM_001206569.2:c.559-76604C>T NP_001193498.1:n.559-76604C>T
NM_001206570.2:c.559-76604C>T NP_001193499.1:n.559-76604C>T
NM_001206571.2:c.559-76604C>T NP_001193500.1:n.559-76604C>T
NM_001206572.2:c.559-76604C>T NP_001193501.1:n.559-76604C>T
NM_052918.5:c.559-76604C>T MANE Select NP_443150.3:n.559-76604C>T
NM_001387556.1:c.559-76604C>T NP_001374485.1:n.559-76604C>T