Canonical Allele Identifier: CA490131551

Gene: TGM5

Linked Data

• gnomAD v4: 15-43252910-C-A
• MyVariant Identifiers: chr15:g.43545108C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252910C>A , CM000677.2:g.43252910C>A	GRCh38
NC_000015.9:g.43545108C>A , CM000677.1:g.43545108C>A	GRCh37
NC_000015.8:g.41332400C>A	NCBI36
NG_016124.1:g.18948G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.711G>T MANE Select	ENSP00000220420.5:p.Val237=
ENST00000635871.1:n.180G>T
ENST00000220420.9:c.711G>T	ENSP00000220420.5:p.Val237=
ENST00000349114.8:c.465G>T	ENSP00000220419.8:p.Val155=
ENST00000610827.4:c.708G>T	ENSP00000479732.1:p.Val236=
ENST00000611276.4:c.462G>T	ENSP00000482542.1:p.Val154=
ENST00000622115.1:c.714G>T	ENSP00000479638.1:p.Val238=
NM_004245.3:c.465G>T	NP_004236.1:p.Val155=
NM_201631.3:c.711G>T	NP_963925.2:p.Val237=
XM_011522229.1:c.711G>T	XP_011520531.1:p.Val237=
XR_931948.1:n.885G>T
NM_004245.4:c.465G>T	NP_004236.1:p.Val155=
NM_201631.4:c.711G>T MANE Select	NP_963925.2:p.Val237=