Canonical Allele Identifier: CA369133394
Gene: TSPAN12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120788686G>A , CM000669.2:g.120788686G>A GRCh38
NC_000007.13:g.120428740G>A , CM000669.1:g.120428740G>A GRCh37
NC_000007.12:g.120215976G>A NCBI36
NG_023203.1:g.74438C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222747.8:c.824C>T MANE Select ENSP00000222747.3:p.Ser275Leu
ENST00000222747.7:c.824C>T ENSP00000222747.3:p.Ser275Leu
ENST00000415871.5:c.824C>T ENSP00000397699.1:p.Ser275Leu
ENST00000450414.5:c.803C>T ENSP00000397411.1:n.803C>T
NM_012338.3:c.824C>T NP_036470.1:p.Ser275Leu
XM_005250239.1:c.824C>T XP_005250296.1:p.Ser275Leu
XM_011515993.1:c.824C>T XP_011514295.1:p.Ser275Leu
XM_011515994.1:c.824C>T XP_011514296.1:p.Ser275Leu
XM_005250239.3:c.824C>T XP_005250296.1:p.Ser275Leu
XM_017011913.1:c.749C>T XP_016867402.1:p.Ser250Leu
NM_012338.4:c.824C>T MANE Select NP_036470.1:p.Ser275Leu