Canonical Allele Identifier: CA2579001894

Gene: TSPAN12

Linked Data

• gnomAD v4: 7-120839940-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120839940A>T , CM000669.2:g.120839940A>T	GRCh38
NC_000007.13:g.120479994A>T , CM000669.1:g.120479994A>T	GRCh37
NC_000007.12:g.120267230A>T	NCBI36
NG_023203.1:g.23184T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.149+87T>A MANE Select	ENSP00000222747.3:n.149+87T>A
ENST00000222747.7:c.149+87T>A	ENSP00000222747.3:n.149+87T>A
ENST00000415871.5:c.149+87T>A	ENSP00000397699.1:n.149+87T>A
ENST00000424710.5:c.149+87T>A	ENSP00000404942.1:n.149+87T>A
ENST00000430985.1:c.149+87T>A	ENSP00000388819.1:n.149+87T>A
ENST00000433758.5:c.149+87T>A	ENSP00000399059.1:n.149+87T>A
ENST00000441017.5:c.149+87T>A	ENSP00000411158.1:n.149+87T>A
NM_012338.3:c.149+87T>A	NP_036470.1:n.149+87T>A
XM_005250239.1:c.149+87T>A	XP_005250296.1:n.149+87T>A
XM_011515993.1:c.149+87T>A	XP_011514295.1:n.149+87T>A
XM_011515994.1:c.149+87T>A	XP_011514296.1:n.149+87T>A
XM_005250239.3:c.149+87T>A	XP_005250296.1:n.149+87T>A
XM_017011913.1:c.149+87T>A	XP_016867402.1:n.149+87T>A
NM_012338.4:c.149+87T>A MANE Select	NP_036470.1:n.149+87T>A