Canonical Allele Identifier: CA369133504

Gene: TSPAN12

Linked Data

• gnomAD v3: 7-120788710-T-G
• gnomAD v4: 7-120788710-T-G
• MyVariant Identifiers: chr7:g.120428764T>G (hg19) ; chr7:g.120788710T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788710T>G , CM000669.2:g.120788710T>G	GRCh38
NC_000007.13:g.120428764T>G , CM000669.1:g.120428764T>G	GRCh37
NC_000007.12:g.120216000T>G	NCBI36
NG_023203.1:g.74414A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.800A>C MANE Select	ENSP00000222747.3:p.Asn267Thr
ENST00000222747.7:c.800A>C	ENSP00000222747.3:p.Asn267Thr
ENST00000415871.5:c.800A>C	ENSP00000397699.1:p.Asn267Thr
ENST00000450414.5:c.779A>C	ENSP00000397411.1:n.779A>C
NM_012338.3:c.800A>C	NP_036470.1:p.Asn267Thr
XM_005250239.1:c.800A>C	XP_005250296.1:p.Asn267Thr
XM_011515993.1:c.800A>C	XP_011514295.1:p.Asn267Thr
XM_011515994.1:c.800A>C	XP_011514296.1:p.Asn267Thr
XM_005250239.3:c.800A>C	XP_005250296.1:p.Asn267Thr
XM_017011913.1:c.725A>C	XP_016867402.1:p.Asn242Thr
NM_012338.4:c.800A>C MANE Select	NP_036470.1:p.Asn267Thr