Canonical Allele Identifier: CA369133518

Gene: TSPAN12

Linked Data

• MyVariant Identifiers: chr7:g.120428767T>G (hg19) ; chr7:g.120788713T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788713T>G , CM000669.2:g.120788713T>G	GRCh38
NC_000007.13:g.120428767T>G , CM000669.1:g.120428767T>G	GRCh37
NC_000007.12:g.120216003T>G	NCBI36
NG_023203.1:g.74411A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.797A>C MANE Select	ENSP00000222747.3:p.Asp266Ala
ENST00000222747.7:c.797A>C	ENSP00000222747.3:p.Asp266Ala
ENST00000415871.5:c.797A>C	ENSP00000397699.1:p.Asp266Ala
ENST00000450414.5:c.776A>C	ENSP00000397411.1:n.776A>C
NM_012338.3:c.797A>C	NP_036470.1:p.Asp266Ala
XM_005250239.1:c.797A>C	XP_005250296.1:p.Asp266Ala
XM_011515993.1:c.797A>C	XP_011514295.1:p.Asp266Ala
XM_011515994.1:c.797A>C	XP_011514296.1:p.Asp266Ala
XM_005250239.3:c.797A>C	XP_005250296.1:p.Asp266Ala
XM_017011913.1:c.722A>C	XP_016867402.1:p.Asp241Ala
NM_012338.4:c.797A>C MANE Select	NP_036470.1:p.Asp266Ala