Canonical Allele Identifier: CA2628101479

Gene: TGM5

Linked Data

• gnomAD v4: 15-43253676-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43253676C>T , CM000677.2:g.43253676C>T	GRCh38
NC_000015.9:g.43545874C>T , CM000677.1:g.43545874C>T	GRCh37
NC_000015.8:g.41333166C>T	NCBI36
NG_016124.1:g.18182G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.556-42G>A MANE Select	ENSP00000220420.5:n.556-42G>A
ENST00000220420.9:c.556-42G>A	ENSP00000220420.5:n.556-42G>A
ENST00000349114.8:c.310-42G>A	ENSP00000220419.8:n.310-42G>A
ENST00000610827.4:c.553-42G>A	ENSP00000479732.1:n.553-42G>A
ENST00000611276.4:c.307-42G>A	ENSP00000482542.1:n.307-42G>A
ENST00000622115.1:c.559-42G>A	ENSP00000479638.1:n.559-42G>A
NM_004245.3:c.310-42G>A	NP_004236.1:n.310-42G>A
NM_201631.3:c.556-42G>A	NP_963925.2:n.556-42G>A
XM_011522229.1:c.556-42G>A	XP_011520531.1:n.556-42G>A
XR_931948.1:n.730-42G>A
NM_004245.4:c.310-42G>A	NP_004236.1:n.310-42G>A
NM_201631.4:c.556-42G>A MANE Select	NP_963925.2:n.556-42G>A