Canonical Allele Identifier: CA577566245

Gene: TSPAN12

Linked Data

• dbSNP Id: rs1475668454
• gnomAD v2: 7-120450673-C-A
• gnomAD v4: 7-120810619-C-A
• MyVariant Identifiers: chr7:g.120450673C>A (hg19) ; chr7:g.120810619C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120810619C>A , CM000669.2:g.120810619C>A	GRCh38
NC_000007.13:g.120450673C>A , CM000669.1:g.120450673C>A	GRCh37
NC_000007.12:g.120237909C>A	NCBI36
NG_023203.1:g.52505G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222747.8:c.361-49G>T MANE Select	ENSP00000222747.3:n.361-49G>T
ENST00000222747.7:c.361-49G>T	ENSP00000222747.3:n.361-49G>T
ENST00000415871.5:c.361-49G>T	ENSP00000397699.1:n.361-49G>T
ENST00000441017.5:c.361-49G>T	ENSP00000411158.1:n.361-49G>T
ENST00000450414.5:c.340-49G>T	ENSP00000397411.1:n.340-49G>T
NM_012338.3:c.361-49G>T	NP_036470.1:n.361-49G>T
XM_005250239.1:c.361-49G>T	XP_005250296.1:n.361-49G>T
XM_011515993.1:c.361-49G>T	XP_011514295.1:n.361-49G>T
XM_011515994.1:c.361-49G>T	XP_011514296.1:n.361-49G>T
XM_005250239.3:c.361-49G>T	XP_005250296.1:n.361-49G>T
XM_017011913.1:c.286-49G>T	XP_016867402.1:n.286-49G>T
NM_012338.4:c.361-49G>T MANE Select	NP_036470.1:n.361-49G>T