Canonical Allele Identifier: CA269975055

Gene: TGM5

Linked Data

• dbSNP Id: rs960071915
• MyVariant Identifiers: chr15:g.43544881A>G (hg19) ; chr15:g.43252683A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252683A>G , CM000677.2:g.43252683A>G	GRCh38
NC_000015.9:g.43544881A>G , CM000677.1:g.43544881A>G	GRCh37
NC_000015.8:g.41332173A>G	NCBI36
NG_016124.1:g.19175T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.862+76T>C MANE Select	ENSP00000220420.5:n.862+76T>C
ENST00000635871.1:n.331+76T>C
ENST00000220420.9:c.862+76T>C	ENSP00000220420.5:n.862+76T>C
ENST00000349114.8:c.616+76T>C	ENSP00000220419.8:n.616+76T>C
ENST00000610827.4:c.859+76T>C	ENSP00000479732.1:n.859+76T>C
ENST00000611276.4:c.613+76T>C	ENSP00000482542.1:n.613+76T>C
ENST00000622115.1:c.865+76T>C	ENSP00000479638.1:n.865+76T>C
NM_004245.3:c.616+76T>C	NP_004236.1:n.616+76T>C
NM_201631.3:c.862+76T>C	NP_963925.2:n.862+76T>C
XM_011522229.1:c.862+76T>C	XP_011520531.1:n.862+76T>C
XR_931948.1:n.1036+76T>C
NM_004245.4:c.616+76T>C	NP_004236.1:n.616+76T>C
NM_201631.4:c.862+76T>C MANE Select	NP_963925.2:n.862+76T>C