Canonical Allele Identifier: CA457393540

Gene: TSPAN12

Linked Data

• dbSNP Id: rs1584917161
• MyVariant Identifiers: chr7:g.120428766G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788712G>A , CM000669.2:g.120788712G>A	GRCh38
NC_000007.13:g.120428766G>A , CM000669.1:g.120428766G>A	GRCh37
NC_000007.12:g.120216002G>A	NCBI36
NG_023203.1:g.74412C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.798C>T MANE Select	ENSP00000222747.3:p.Asp266=
ENST00000222747.7:c.798C>T	ENSP00000222747.3:p.Asp266=
ENST00000415871.5:c.798C>T	ENSP00000397699.1:p.Asp266=
ENST00000450414.5:c.777C>T	ENSP00000397411.1:n.777C>T
NM_012338.3:c.798C>T	NP_036470.1:p.Asp266=
XM_005250239.1:c.798C>T	XP_005250296.1:p.Asp266=
XM_011515993.1:c.798C>T	XP_011514295.1:p.Asp266=
XM_011515994.1:c.798C>T	XP_011514296.1:p.Asp266=
XM_005250239.3:c.798C>T	XP_005250296.1:p.Asp266=
XM_017011913.1:c.723C>T	XP_016867402.1:p.Asp241=
NM_012338.4:c.798C>T MANE Select	NP_036470.1:p.Asp266=