Canonical Allele Identifier: CA14756247

Gene: TGM2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.38155180T>C , CM000682.2:g.38155180T>C	GRCh38
NC_000020.10:g.36783582T>C , CM000682.1:g.36783582T>C	GRCh37
NC_000020.9:g.36216996T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361475.7:c.433+667A>G MANE Select	ENSP00000355330.2:n.433+667A>G
ENST00000361475.6:c.433+667A>G	ENSP00000355330.2:n.433+667A>G
ENST00000373403.7:c.433+667A>G	ENSP00000362502.3:n.433+667A>G
ENST00000453095.1:c.433+667A>G	ENSP00000387642.1:n.433+667A>G
ENST00000468262.5:n.517+667A>G
ENST00000474777.1:n.494+667A>G
NM_004613.2:c.433+667A>G	NP_004604.2:n.433+667A>G
NM_198951.1:c.433+667A>G	NP_945189.1:n.433+667A>G
XM_011529028.1:c.433+667A>G	XP_011527330.1:n.433+667A>G
XM_011529029.1:c.433+667A>G	XP_011527331.1:n.433+667A>G
NM_001323316.1:c.433+667A>G	NP_001310245.1:n.433+667A>G
NM_001323317.1:c.191-4123A>G	NP_001310246.1:n.191-4123A>G
NM_001323318.1:c.253+667A>G	NP_001310247.1:n.253+667A>G
NM_004613.3:c.433+667A>G	NP_004604.2:n.433+667A>G
NM_198951.2:c.433+667A>G	NP_945189.1:n.433+667A>G
NM_004613.4:c.433+667A>G MANE Select	NP_004604.2:n.433+667A>G
NM_001323316.2:c.433+667A>G	NP_001310245.1:n.433+667A>G
NM_001323317.2:c.191-4123A>G	NP_001310246.1:n.191-4123A>G
NM_001323318.2:c.253+667A>G	NP_001310247.1:n.253+667A>G
NM_198951.3:c.433+667A>G	NP_945189.1:n.433+667A>G