Canonical Allele Identifier: CA1348101132
Gene: DAZL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.16598084C= , CM000665.2:g.16598084C= GRCh38
NC_000003.11:g.16639591C= , CM000665.1:g.16639591C= GRCh37
NC_000003.10:g.16614595C= NCBI36
NG_023329.1:g.12416G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399444.7:c.242+3G= MANE Select ENSP00000382373.3:n.242+3G=
ENST00000250863.12:c.302+3G= ENSP00000250863.8:n.302+3G=
ENST00000399444.6:c.242+3G= ENSP00000382373.2:n.242+3G=
ENST00000454457.1:c.356+3G= ENSP00000398109.1:n.356+3G=
NM_001190811.1:c.302+3G= NP_001177740.1:n.302+3G=
NM_001351.3:c.242+3G= NP_001342.2:n.242+3G=
NM_001351.4:c.242+3G= MANE Select NP_001342.2:n.242+3G=
NM_001190811.2:c.302+3G= NP_001177740.1:n.302+3G=
Search 100 bp 5'
Search 100 bp 3'