Canonical Allele Identifier: CA1738876096

Gene: TSPAN12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788604C= , CM000669.2:g.120788604C=	GRCh38
NC_000007.13:g.120428658C= , CM000669.1:g.120428658C=	GRCh37
NC_000007.12:g.120215894C=	NCBI36
NG_023203.1:g.74520G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222747.8:c.906G= MANE Select	ENSP00000222747.3:p.Met302=
ENST00000222747.7:c.906G=	ENSP00000222747.3:p.Met302=
ENST00000415871.5:c.906G=	ENSP00000397699.1:p.Met302=
ENST00000450414.5:c.885G=	ENSP00000397411.1:n.885G=
NM_012338.3:c.906G=	NP_036470.1:p.Met302=
XM_005250239.1:c.906G=	XP_005250296.1:p.Met302=
XM_011515993.1:c.906G=	XP_011514295.1:p.Met302=
XM_011515994.1:c.906G=	XP_011514296.1:p.Met302=
XM_005250239.3:c.906G=	XP_005250296.1:p.Met302=
XM_017011913.1:c.831G=	XP_016867402.1:p.Met277=
NM_012338.4:c.906G= MANE Select	NP_036470.1:p.Met302=