Canonical Allele Identifier: CA2448039163

Gene: TNMD

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100596679C>A , CM000685.2:g.100596679C>A	GRCh38
NC_000023.10:g.99851676C>A , CM000685.1:g.99851676C>A	GRCh37
NC_000023.9:g.99738332C>A	NCBI36
NG_013266.1:g.16887C>A
NG_013266.2:g.16887C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373031.5:c.424-825C>A MANE Select	ENSP00000362122.4:n.424-825C>A
ENST00000373031.4:c.424-825C>A	ENSP00000362122.4:n.424-825C>A
ENST00000485971.1:n.515-825C>A
NM_022144.2:c.424-825C>A	NP_071427.2:n.424-825C>A
XM_005262175.3:c.235-825C>A	XP_005262232.1:n.235-825C>A
XM_005262176.1:c.424-825C>A	XP_005262233.1:n.424-825C>A
XM_011531008.1:c.235-825C>A	XP_011529310.1:n.235-825C>A
XM_011531009.1:c.235-825C>A	XP_011529311.1:n.235-825C>A
XM_011531010.1:c.235-825C>A	XP_011529312.1:n.235-825C>A
NM_022144.3:c.424-825C>A MANE Select	NP_071427.2:n.424-825C>A