Canonical Allele Identifier: CA392091763

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43531025C>A (hg19) ; chr15:g.43238827C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43238827C>A , CM000677.2:g.43238827C>A	GRCh38
NC_000015.9:g.43531025C>A , CM000677.1:g.43531025C>A	GRCh37
NC_000015.8:g.41318317C>A	NCBI36
NG_016124.1:g.33031G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.1335G>T MANE Select	ENSP00000220420.5:p.Lys445Asn
ENST00000220420.9:c.1335G>T	ENSP00000220420.5:p.Lys445Asn
ENST00000349114.8:c.1089G>T	ENSP00000220419.8:p.Lys363Asn
ENST00000396996.3:n.811G>T
ENST00000610827.4:c.1332G>T	ENSP00000479732.1:p.Lys444Asn
ENST00000611276.4:c.1086G>T	ENSP00000482542.1:p.Lys362Asn
ENST00000622115.1:c.1338G>T	ENSP00000479638.1:p.Lys446Asn
NM_004245.3:c.1089G>T	NP_004236.1:p.Lys363Asn
NM_201631.3:c.1335G>T	NP_963925.2:p.Lys445Asn
XM_011522229.1:c.1335G>T	XP_011520531.1:p.Lys445Asn
XM_011522230.1:c.306G>T	XP_011520532.1:p.Lys102Asn
XR_931948.1:n.1509G>T
XM_011522230.2:c.306G>T	XP_011520532.1:p.Lys102Asn
XM_017022729.1:c.306G>T	XP_016878218.1:p.Lys102Asn
NM_004245.4:c.1089G>T	NP_004236.1:p.Lys363Asn
NM_201631.4:c.1335G>T MANE Select	NP_963925.2:p.Lys445Asn