Canonical Allele Identifier: CA31272860
Gene: SPTA1 HGNC NCBI

Linked Data

dbSNP Id: rs926813031

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158685415T>C , CM000663.2:g.158685415T>C GRCh38
NC_000001.10:g.158655205T>C , CM000663.1:g.158655205T>C GRCh37
NC_000001.9:g.156921829T>C NCBI36
NG_011474.1:g.6302A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000643759.2:c.25-68A>G MANE Select ENSP00000495214.1:n.25-68A>G
ENST00000368147.8:c.25-68A>G ENSP00000357129.4:n.25-68A>G
ENST00000467387.1:c.25-68A>G ENSP00000476485.1:n.25-68A>G
ENST00000614909.4:c.25-68A>G ENSP00000482595.1:n.25-68A>G
NM_003126.2:c.25-68A>G NP_003117.2:n.25-68A>G
XM_011509916.1:c.25-68A>G XP_011508218.1:n.25-68A>G
XM_011509917.1:c.25-68A>G XP_011508219.1:n.25-68A>G
XM_011509918.1:c.25-68A>G XP_011508220.1:n.25-68A>G
XM_011509919.1:c.25-68A>G XP_011508221.1:n.25-68A>G
XR_921911.1:n.138-68A>G
XR_921912.1:n.143-68A>G
NM_003126.3:c.25-68A>G NP_003117.2:n.25-68A>G
XM_011509916.2:c.25-68A>G XP_011508218.1:n.25-68A>G
XM_011509917.3:c.25-68A>G XP_011508219.1:n.25-68A>G
XM_011509918.3:c.25-68A>G XP_011508220.1:n.25-68A>G
XM_011509919.3:c.25-68A>G XP_011508221.1:n.25-68A>G
XR_921911.3:n.151-68A>G
XR_921912.2:n.153-68A>G
NM_003126.4:c.25-68A>G MANE Select NP_003117.2:n.25-68A>G