Canonical Allele Identifier: CA2652806501

Gene: TGM2

Linked Data

• gnomAD v4: 20-38165136-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.38165136C>T , CM000682.2:g.38165136C>T	GRCh38
NC_000020.10:g.36793538C>T , CM000682.1:g.36793538C>T	GRCh37
NC_000020.9:g.36226952C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361475.7:c.10+53G>A MANE Select	ENSP00000355330.2:n.10+53G>A
ENST00000361475.6:c.10+53G>A	ENSP00000355330.2:n.10+53G>A
ENST00000373403.7:c.10+53G>A	ENSP00000362502.3:n.10+53G>A
ENST00000453095.1:c.10+53G>A	ENSP00000387642.1:n.10+53G>A
ENST00000468262.5:n.94+53G>A
ENST00000474777.1:n.71+53G>A
NM_004613.2:c.10+53G>A	NP_004604.2:n.10+53G>A
NM_198951.1:c.10+53G>A	NP_945189.1:n.10+53G>A
XM_011529028.1:c.10+53G>A	XP_011527330.1:n.10+53G>A
XM_011529029.1:c.10+53G>A	XP_011527331.1:n.10+53G>A
NM_001323316.1:c.10+53G>A	NP_001310245.1:n.10+53G>A
NM_001323317.1:c.10+53G>A	NP_001310246.1:n.10+53G>A
NM_001323318.1:c.10+53G>A	NP_001310247.1:n.10+53G>A
NM_004613.3:c.10+53G>A	NP_004604.2:n.10+53G>A
NM_198951.2:c.10+53G>A	NP_945189.1:n.10+53G>A
XR_001754586.1:n.43G>A
NM_004613.4:c.10+53G>A MANE Select	NP_004604.2:n.10+53G>A
NM_001323316.2:c.10+53G>A	NP_001310245.1:n.10+53G>A
NM_001323317.2:c.10+53G>A	NP_001310246.1:n.10+53G>A
NM_001323318.2:c.10+53G>A	NP_001310247.1:n.10+53G>A
NM_198951.3:c.10+53G>A	NP_945189.1:n.10+53G>A