Canonical Allele Identifier: CA369137482

Gene: TSPAN12

Linked Data

• MyVariant Identifiers: chr7:g.120450575T>G (hg19) ; chr7:g.120810521T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120810521T>G , CM000669.2:g.120810521T>G	GRCh38
NC_000007.13:g.120450575T>G , CM000669.1:g.120450575T>G	GRCh37
NC_000007.12:g.120237811T>G	NCBI36
NG_023203.1:g.52603A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.410A>C MANE Select	ENSP00000222747.3:p.Asn137Thr
ENST00000222747.7:c.410A>C	ENSP00000222747.3:p.Asn137Thr
ENST00000415871.5:c.410A>C	ENSP00000397699.1:p.Asn137Thr
ENST00000441017.5:c.410A>C	ENSP00000411158.1:p.Asn137Thr
ENST00000450414.5:c.389A>C	ENSP00000397411.1:n.389A>C
NM_012338.3:c.410A>C	NP_036470.1:p.Asn137Thr
XM_005250239.1:c.410A>C	XP_005250296.1:p.Asn137Thr
XM_011515993.1:c.410A>C	XP_011514295.1:p.Asn137Thr
XM_011515994.1:c.410A>C	XP_011514296.1:p.Asn137Thr
XM_005250239.3:c.410A>C	XP_005250296.1:p.Asn137Thr
XM_017011913.1:c.335A>C	XP_016867402.1:p.Asn112Thr
NM_012338.4:c.410A>C MANE Select	NP_036470.1:p.Asn137Thr