Canonical Allele Identifier: CA2467003795
Gene: TMLHE HGNC NCBI

Linked Data

dbSNP Id: rs2067073479

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155505913G>A , CM000685.2:g.155505913G>A GRCh38
NC_000023.10:g.154735574G>A , CM000685.1:g.154735574G>A GRCh37
NC_000023.9:g.154388768G>A NCBI36
NG_021318.1:g.112049C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334398.8:c.995+985C>T MANE Select ENSP00000335261.3:n.995+985C>T
ENST00000675642.1:c.1028+985C>T ENSP00000502604.1:n.1028+985C>T
ENST00000334398.7:c.995+985C>T ENSP00000335261.3:n.995+985C>T
ENST00000369439.4:c.995+985C>T ENSP00000358447.4:n.995+985C>T
NM_001184797.1:c.995+985C>T NP_001171726.1:n.995+985C>T
NM_018196.3:c.995+985C>T NP_060666.1:n.995+985C>T
XM_011531182.1:c.842+985C>T XP_011529484.1:n.842+985C>T
XR_247318.1:n.1166+985C>T
XM_011531182.3:c.842+985C>T XP_011529484.1:n.842+985C>T
XR_247318.3:n.1140+985C>T
NM_018196.4:c.995+985C>T MANE Select NP_060666.1:n.995+985C>T
NM_001184797.2:c.995+985C>T NP_001171726.1:n.995+985C>T