Canonical Allele Identifier: CA343011466
Gene: SPTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158612895C>A , CM000663.2:g.158612895C>A GRCh38
NC_000001.10:g.158582685C>A , CM000663.1:g.158582685C>A GRCh37
NC_000001.9:g.156849309C>A NCBI36
NG_011474.1:g.78822G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643759.2:c.7056G>T MANE Select ENSP00000495214.1:p.Lys2352Asn
ENST00000368147.8:c.7056G>T ENSP00000357129.4:p.Lys2352Asn
ENST00000481212.5:n.497G>T
ENST00000498708.1:n.488G>T
ENST00000614909.4:c.7056G>T ENSP00000482595.1:p.Lys2352Asn
NM_003126.2:c.7056G>T NP_003117.2:p.Lys2352Asn
XM_011509916.1:c.7056G>T XP_011508218.1:p.Lys2352Asn
XM_011509917.1:c.7038G>T XP_011508219.1:p.Lys2346Asn
NM_003126.3:c.7056G>T NP_003117.2:p.Lys2352Asn
XM_011509916.2:c.7056G>T XP_011508218.1:p.Lys2352Asn
XM_011509917.3:c.7038G>T XP_011508219.1:p.Lys2346Asn
NM_003126.4:c.7056G>T MANE Select NP_003117.2:p.Lys2352Asn