Canonical Allele Identifier: CA358669
Community Standard Title: NM_018196.4(TMLHE):c.1107G>T (p.Glu369Asp)
Gene: TMLHE HGNC NCBI
TMLHE-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155492384C>A , CM000685.2:g.155492384C>A GRCh38
NC_000023.10:g.154722045C>A , CM000685.1:g.154722045C>A GRCh37
NC_000023.9:g.154375239C>A NCBI36
NG_021318.1:g.125578G>T

Transcript Alleles

HGVS Amino-acid Change
NM_018196.4:c.1107G>T (TMLHE) MANE Select NP_060666.1:p.Glu369Asp
ENST00000334398.8:c.1107G>T (TMLHE) MANE Select ENSP00000335261.3:p.Glu369Asp
NM_018196.3:c.1107G>T (TMLHE) NP_060666.1:p.Glu369Asp
NR_039991.1:n.472-496C>A (TMLHE-AS1)
ENST00000334398.7:c.1107G>T (TMLHE) ENSP00000335261.3:p.Glu369Asp
ENST00000449645.2:n.106G>T (TMLHE)
ENST00000675642.1:c.1140G>T (TMLHE) ENSP00000502604.1:p.Glu380Asp
XM_011531182.1:c.954G>T (TMLHE) XP_011529484.1:p.Glu318Asp
XM_011531182.3:c.954G>T (TMLHE) XP_011529484.1:p.Glu318Asp
XR_247318.1:n.1278G>T (TMLHE)
XR_247318.3:n.1252G>T (TMLHE)