Canonical Allele Identifier: CA2628100776

Gene: TGM5

Linked Data

• gnomAD v4: 15-43252663-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252663G>T , CM000677.2:g.43252663G>T	GRCh38
NC_000015.9:g.43544861G>T , CM000677.1:g.43544861G>T	GRCh37
NC_000015.8:g.41332153G>T	NCBI36
NG_016124.1:g.19195C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.862+96C>A MANE Select	ENSP00000220420.5:n.862+96C>A
ENST00000635871.1:n.331+96C>A
ENST00000220420.9:c.862+96C>A	ENSP00000220420.5:n.862+96C>A
ENST00000349114.8:c.616+96C>A	ENSP00000220419.8:n.616+96C>A
ENST00000610827.4:c.859+96C>A	ENSP00000479732.1:n.859+96C>A
ENST00000611276.4:c.613+96C>A	ENSP00000482542.1:n.613+96C>A
ENST00000622115.1:c.865+96C>A	ENSP00000479638.1:n.865+96C>A
NM_004245.3:c.616+96C>A	NP_004236.1:n.616+96C>A
NM_201631.3:c.862+96C>A	NP_963925.2:n.862+96C>A
XM_011522229.1:c.862+96C>A	XP_011520531.1:n.862+96C>A
XR_931948.1:n.1036+96C>A
NM_004245.4:c.616+96C>A	NP_004236.1:n.616+96C>A
NM_201631.4:c.862+96C>A MANE Select	NP_963925.2:n.862+96C>A