Canonical Allele Identifier: CA13274751

Gene: SORCS1

Linked Data

• dbSNP Id: rs950809
• gnomAD v2: 10-108795375-A-G
• gnomAD v3: 10-107035617-A-G
• gnomAD v4: 10-107035617-A-G
• MyVariant Identifiers: chr10:g.108795375A>G (hg19) ; chr10:g.107035617A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.107035617A>G , CM000672.2:g.107035617A>G	GRCh38
NC_000010.10:g.108795375A>G , CM000672.1:g.108795375A>G	GRCh37
NC_000010.9:g.108785365A>G	NCBI36
NG_029120.1:g.134092T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263054.11:c.559-79037T>C MANE Select	ENSP00000263054.5:n.559-79037T>C
ENST00000263054.10:c.559-79037T>C	ENSP00000263054.5:n.559-79037T>C
NM_001013031.2:c.559-79037T>C	NP_001013049.1:n.559-79037T>C
NM_001206569.1:c.559-79037T>C	NP_001193498.1:n.559-79037T>C
NM_001206570.1:c.559-79037T>C	NP_001193499.1:n.559-79037T>C
NM_001206571.1:c.559-79037T>C	NP_001193500.1:n.559-79037T>C
NM_001206572.1:c.559-79037T>C	NP_001193501.1:n.559-79037T>C
NM_052918.4:c.559-79037T>C	NP_443150.3:n.559-79037T>C
XM_011539199.1:c.559-79037T>C	XP_011537501.1:n.559-79037T>C
XM_011539200.1:c.559-79037T>C	XP_011537502.1:n.559-79037T>C
XM_011539201.1:c.559-79037T>C	XP_011537503.1:n.559-79037T>C
XM_011539204.1:c.4-79037T>C	XP_011537506.1:n.4-79037T>C
XM_011539206.1:c.559-79037T>C	XP_011537508.1:n.559-79037T>C
XM_011539199.3:c.559-79037T>C	XP_011537501.1:n.559-79037T>C
XM_011539201.3:c.559-79037T>C	XP_011537503.1:n.559-79037T>C
XM_017015614.2:c.559-79037T>C	XP_016871103.1:n.559-79037T>C
XM_017015615.2:c.559-79037T>C	XP_016871104.1:n.559-79037T>C
XM_017015617.1:c.4-79037T>C	XP_016871106.1:n.4-79037T>C
NM_001013031.3:c.559-79037T>C	NP_001013049.1:n.559-79037T>C
NM_001206569.2:c.559-79037T>C	NP_001193498.1:n.559-79037T>C
NM_001206570.2:c.559-79037T>C	NP_001193499.1:n.559-79037T>C
NM_001206571.2:c.559-79037T>C	NP_001193500.1:n.559-79037T>C
NM_001206572.2:c.559-79037T>C	NP_001193501.1:n.559-79037T>C
NM_052918.5:c.559-79037T>C MANE Select	NP_443150.3:n.559-79037T>C
NM_001387556.1:c.559-79037T>C	NP_001374485.1:n.559-79037T>C