Canonical Allele Identifier: CA2841600220

Gene: TSPAN12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120810581A>G , CM000669.2:g.120810581A>G	GRCh38
NC_000007.13:g.120450635A>G , CM000669.1:g.120450635A>G	GRCh37
NC_000007.12:g.120237871A>G	NCBI36
NG_023203.1:g.52543T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222747.8:c.361-11T>C MANE Select	ENSP00000222747.3:n.361-11T>C
ENST00000222747.7:c.361-11T>C	ENSP00000222747.3:n.361-11T>C
ENST00000415871.5:c.361-11T>C	ENSP00000397699.1:n.361-11T>C
ENST00000441017.5:c.361-11T>C	ENSP00000411158.1:n.361-11T>C
ENST00000450414.5:c.340-11T>C	ENSP00000397411.1:n.340-11T>C
NM_012338.3:c.361-11T>C	NP_036470.1:n.361-11T>C
XM_005250239.1:c.361-11T>C	XP_005250296.1:n.361-11T>C
XM_011515993.1:c.361-11T>C	XP_011514295.1:n.361-11T>C
XM_011515994.1:c.361-11T>C	XP_011514296.1:n.361-11T>C
XM_005250239.3:c.361-11T>C	XP_005250296.1:n.361-11T>C
XM_017011913.1:c.286-11T>C	XP_016867402.1:n.286-11T>C
NM_012338.4:c.361-11T>C MANE Select	NP_036470.1:n.361-11T>C