Canonical Allele Identifier: CA10913173
Gene: DTL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212064456G>A , CM000663.2:g.212064456G>A GRCh38
NC_000001.10:g.212237798G>A , CM000663.1:g.212237798G>A GRCh37
NC_000001.9:g.210304421G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366991.5:c.527-461G>A MANE Select ENSP00000355958.4:n.527-461G>A
ENST00000366991.4:c.527-461G>A ENSP00000355958.4:n.527-461G>A
ENST00000475419.5:n.446-461G>A
ENST00000542077.5:c.401-461G>A ENSP00000443870.1:n.401-461G>A
NM_001286229.1:c.-183-461G>A NP_001273158.1:n.-183-461G>A
NM_001286230.1:c.401-461G>A NP_001273159.1:n.401-461G>A
NM_016448.3:c.527-461G>A NP_057532.3:n.527-461G>A
XM_011509614.1:c.341-461G>A XP_011507916.1:n.341-461G>A
NM_016448.4:c.527-461G>A MANE Select NP_057532.4:n.527-461G>A
NM_001286229.2:c.-183-461G>A NP_001273158.2:n.-183-461G>A
NM_001286230.2:c.401-461G>A NP_001273159.2:n.401-461G>A
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