Canonical Allele Identifier: CA369133181

Gene: TSPAN12

Linked Data

• MyVariant Identifiers: chr7:g.120428660T>C (hg19) ; chr7:g.120788606T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788606T>C , CM000669.2:g.120788606T>C	GRCh38
NC_000007.13:g.120428660T>C , CM000669.1:g.120428660T>C	GRCh37
NC_000007.12:g.120215896T>C	NCBI36
NG_023203.1:g.74518A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222747.8:c.904A>G MANE Select	ENSP00000222747.3:p.Met302Val
ENST00000222747.7:c.904A>G	ENSP00000222747.3:p.Met302Val
ENST00000415871.5:c.904A>G	ENSP00000397699.1:p.Met302Val
ENST00000450414.5:c.883A>G	ENSP00000397411.1:n.883A>G
NM_012338.3:c.904A>G	NP_036470.1:p.Met302Val
XM_005250239.1:c.904A>G	XP_005250296.1:p.Met302Val
XM_011515993.1:c.904A>G	XP_011514295.1:p.Met302Val
XM_011515994.1:c.904A>G	XP_011514296.1:p.Met302Val
XM_005250239.3:c.904A>G	XP_005250296.1:p.Met302Val
XM_017011913.1:c.829A>G	XP_016867402.1:p.Met277Val
NM_012338.4:c.904A>G MANE Select	NP_036470.1:p.Met302Val