Canonical Allele Identifier: CA2610725099

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102836673-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102836673T>G , CM000672.2:g.102836673T>G	GRCh38
NC_000010.10:g.104596430T>G , CM000672.1:g.104596430T>G	GRCh37
NC_000010.9:g.104586420T>G	NCBI36
NG_007955.1:g.5861A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.297+392A>C MANE Select	ENSP00000358903.3:n.297+392A>C
ENST00000638190.1:c.297+392A>C	ENSP00000492539.1:n.297+392A>C
ENST00000638272.1:c.297+392A>C	ENSP00000491508.1:n.297+392A>C
ENST00000638971.1:c.297+392A>C	ENSP00000492313.1:n.297+392A>C
ENST00000639393.1:c.297+392A>C	ENSP00000492651.1:n.297+392A>C
ENST00000640633.1:n.59+41A>C
ENST00000369887.3:c.297+392A>C	ENSP00000358903.3:n.297+392A>C
ENST00000489268.1:n.350+392A>C
NM_000102.3:c.297+392A>C	NP_000093.1:n.297+392A>C
NM_000102.4:c.297+392A>C MANE Select	NP_000093.1:n.297+392A>C