Canonical Allele Identifier: CA2467003811

Gene: TMLHE

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155505950T= , CM000685.2:g.155505950T=	GRCh38
NC_000023.10:g.154735611T= , CM000685.1:g.154735611T=	GRCh37
NC_000023.9:g.154388805T=	NCBI36
NG_021318.1:g.112012A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334398.8:c.995+948A= MANE Select	ENSP00000335261.3:n.995+948A=
ENST00000675642.1:c.1028+948A=	ENSP00000502604.1:n.1028+948A=
ENST00000334398.7:c.995+948A=	ENSP00000335261.3:n.995+948A=
ENST00000369439.4:c.995+948A=	ENSP00000358447.4:n.995+948A=
NM_001184797.1:c.995+948A=	NP_001171726.1:n.995+948A=
NM_018196.3:c.995+948A=	NP_060666.1:n.995+948A=
XM_011531182.1:c.842+948A=	XP_011529484.1:n.842+948A=
XR_247318.1:n.1166+948A=
XM_011531182.3:c.842+948A=	XP_011529484.1:n.842+948A=
XR_247318.3:n.1140+948A=
NM_018196.4:c.995+948A= MANE Select	NP_060666.1:n.995+948A=
NM_001184797.2:c.995+948A=	NP_001171726.1:n.995+948A=