Canonical Allele Identifier: CA832470401

Gene: TSPAN12

Linked Data

• dbSNP Id: rs1171200664
• MyVariant Identifiers: chr7:g.120480068del (hg19) ; chr7:g.120840014del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120840015del , CM000669.2:g.120840015del	GRCh38
NC_000007.13:g.120480069del , CM000669.1:g.120480069del	GRCh37
NC_000007.12:g.120267305del	NCBI36
NG_023203.1:g.23110del

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.149+13del MANE Select	ENSP00000222747.3:n.149+13del
ENST00000222747.7:c.149+13del	ENSP00000222747.3:n.149+13del
ENST00000415871.5:c.149+13del	ENSP00000397699.1:n.149+13del
ENST00000424710.5:c.149+13del	ENSP00000404942.1:n.149+13del
ENST00000430985.1:c.149+13del	ENSP00000388819.1:n.149+13del
ENST00000433758.5:c.149+13del	ENSP00000399059.1:n.149+13del
ENST00000441017.5:c.149+13del	ENSP00000411158.1:n.149+13del
NM_012338.3:c.149+13del	NP_036470.1:n.149+13del
XM_005250239.1:c.149+13del	XP_005250296.1:n.149+13del
XM_011515993.1:c.149+13del	XP_011514295.1:n.149+13del
XM_011515994.1:c.149+13del	XP_011514296.1:n.149+13del
XM_005250239.3:c.149+13del	XP_005250296.1:n.149+13del
XM_017011913.1:c.149+13del	XP_016867402.1:n.149+13del
NM_012338.4:c.149+13del MANE Select	NP_036470.1:n.149+13del