Canonical Allele Identifier: CA343011127
Gene: SPTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158612836G>C , CM000663.2:g.158612836G>C GRCh38
NC_000001.10:g.158582626G>C , CM000663.1:g.158582626G>C GRCh37
NC_000001.9:g.156849250G>C NCBI36
NG_011474.1:g.78881C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000643759.2:c.7115C>G MANE Select ENSP00000495214.1:p.Thr2372Ser
ENST00000368147.8:c.7115C>G ENSP00000357129.4:p.Thr2372Ser
ENST00000481212.5:n.556C>G
ENST00000498708.1:n.547C>G
ENST00000614909.4:c.7115C>G ENSP00000482595.1:p.Thr2372Ser
NM_003126.2:c.7115C>G NP_003117.2:p.Thr2372Ser
XM_011509916.1:c.7115C>G XP_011508218.1:p.Thr2372Ser
XM_011509917.1:c.7097C>G XP_011508219.1:p.Thr2366Ser
NM_003126.3:c.7115C>G NP_003117.2:p.Thr2372Ser
XM_011509916.2:c.7115C>G XP_011508218.1:p.Thr2372Ser
XM_011509917.3:c.7097C>G XP_011508219.1:p.Thr2366Ser
NM_003126.4:c.7115C>G MANE Select NP_003117.2:p.Thr2372Ser