Canonical Allele Identifier: CA948015980
Community Standard Title: NM_003920.5(TIMELESS):c.-62+4349C>A
Gene: TIMELESS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56444961G>T , CM000674.2:g.56444961G>T GRCh38
NC_000012.11:g.56838745G>T , CM000674.1:g.56838745G>T GRCh37
NC_000012.10:g.55125012G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_003920.5:c.-62+4349C>A MANE Select NP_003911.2:n.-62+4349C>A
ENST00000553532.6:c.-62+4349C>A MANE Select ENSP00000450607.1:n.-62+4349C>A
NM_001330295.1:c.-62+4349C>A NP_001317224.1:n.-62+4349C>A
NM_001330295.2:c.-62+4349C>A NP_001317224.1:n.-62+4349C>A
NM_003920.3:c.-62+4349C>A NP_003911.2:n.-62+4349C>A
NM_003920.4:c.-62+4349C>A NP_003911.2:n.-62+4349C>A
NR_138471.1:n.156+4349C>A
NR_138471.2:n.117+4349C>A
ENST00000229201.4:c.-62+4349C>A ENSP00000229201.4:n.-62+4349C>A
ENST00000553532.5:c.-62+4349C>A ENSP00000450607.1:n.-62+4349C>A
XM_011538939.1:c.-62+4349C>A XP_011537241.1:n.-62+4349C>A