Canonical Allele Identifier: CA432673659
Gene: DAZL HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.16639599G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.16598092G>C , CM000665.2:g.16598092G>C GRCh38
NC_000003.11:g.16639599G>C , CM000665.1:g.16639599G>C GRCh37
NC_000003.10:g.16614603G>C NCBI36
NG_023329.1:g.12408C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399444.7:c.237C>G MANE Select ENSP00000382373.3:p.Ser79=
ENST00000250863.12:c.297C>G ENSP00000250863.8:p.Ser99=
ENST00000399444.6:c.237C>G ENSP00000382373.2:p.Ser79=
ENST00000454457.1:c.351C>G ENSP00000398109.1:p.Ser117=
NM_001190811.1:c.297C>G NP_001177740.1:p.Ser99=
NM_001351.3:c.237C>G NP_001342.2:p.Ser79=
NM_001351.4:c.237C>G MANE Select NP_001342.2:p.Ser79=
NM_001190811.2:c.297C>G NP_001177740.1:p.Ser99=