Canonical Allele Identifier: CA2610725419
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102836914-AAGGTTCACTCCCTTCACATCATCCCACTAGTCTACTTTG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102836915_102836953del , CM000672.2:g.102836915_102836953del GRCh38
NC_000010.10:g.104596672_104596710del , CM000672.1:g.104596672_104596710del GRCh37
NC_000010.9:g.104586662_104586700del NCBI36
NG_007955.1:g.5581_5619del

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.297+112_297+150del MANE Select ENSP00000358903.3:n.297+112_297+150del
ENST00000638190.1:c.297+112_297+150del ENSP00000492539.1:n.297+112_297+150del
ENST00000638272.1:c.297+112_297+150del ENSP00000491508.1:n.297+112_297+150del
ENST00000638971.1:c.297+112_297+150del ENSP00000492313.1:n.297+112_297+150del
ENST00000639393.1:c.297+112_297+150del ENSP00000492651.1:n.297+112_297+150del
ENST00000369887.3:c.297+112_297+150del ENSP00000358903.3:n.297+112_297+150del
ENST00000489268.1:n.350+112_350+150del
NM_000102.3:c.297+112_297+150del NP_000093.1:n.297+112_297+150del
NM_000102.4:c.297+112_297+150del MANE Select NP_000093.1:n.297+112_297+150del
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