Canonical Allele Identifier: CA2684648818

Gene: TSPAN12

Linked Data

• gnomAD v4: 7-120839941-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120839941A>G , CM000669.2:g.120839941A>G	GRCh38
NC_000007.13:g.120479995A>G , CM000669.1:g.120479995A>G	GRCh37
NC_000007.12:g.120267231A>G	NCBI36
NG_023203.1:g.23183T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.149+86T>C MANE Select	ENSP00000222747.3:n.149+86T>C
ENST00000222747.7:c.149+86T>C	ENSP00000222747.3:n.149+86T>C
ENST00000415871.5:c.149+86T>C	ENSP00000397699.1:n.149+86T>C
ENST00000424710.5:c.149+86T>C	ENSP00000404942.1:n.149+86T>C
ENST00000430985.1:c.149+86T>C	ENSP00000388819.1:n.149+86T>C
ENST00000433758.5:c.149+86T>C	ENSP00000399059.1:n.149+86T>C
ENST00000441017.5:c.149+86T>C	ENSP00000411158.1:n.149+86T>C
NM_012338.3:c.149+86T>C	NP_036470.1:n.149+86T>C
XM_005250239.1:c.149+86T>C	XP_005250296.1:n.149+86T>C
XM_011515993.1:c.149+86T>C	XP_011514295.1:n.149+86T>C
XM_011515994.1:c.149+86T>C	XP_011514296.1:n.149+86T>C
XM_005250239.3:c.149+86T>C	XP_005250296.1:n.149+86T>C
XM_017011913.1:c.149+86T>C	XP_016867402.1:n.149+86T>C
NM_012338.4:c.149+86T>C MANE Select	NP_036470.1:n.149+86T>C