Canonical Allele Identifier: CA392100790

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43545748G>C (hg19) ; chr15:g.43253550G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43253550G>C , CM000677.2:g.43253550G>C	GRCh38
NC_000015.9:g.43545748G>C , CM000677.1:g.43545748G>C	GRCh37
NC_000015.8:g.41333040G>C	NCBI36
NG_016124.1:g.18308C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.640C>G MANE Select	ENSP00000220420.5:p.Leu214Val
ENST00000635871.1:n.109C>G
ENST00000220420.9:c.640C>G	ENSP00000220420.5:p.Leu214Val
ENST00000349114.8:c.394C>G	ENSP00000220419.8:p.Leu132Val
ENST00000610827.4:c.637C>G	ENSP00000479732.1:p.Leu213Val
ENST00000611276.4:c.391C>G	ENSP00000482542.1:p.Leu131Val
ENST00000622115.1:c.643C>G	ENSP00000479638.1:p.Leu215Val
NM_004245.3:c.394C>G	NP_004236.1:p.Leu132Val
NM_201631.3:c.640C>G	NP_963925.2:p.Leu214Val
XM_011522229.1:c.640C>G	XP_011520531.1:p.Leu214Val
XR_931948.1:n.814C>G
NM_004245.4:c.394C>G	NP_004236.1:p.Leu132Val
NM_201631.4:c.640C>G MANE Select	NP_963925.2:p.Leu214Val