Canonical Allele Identifier: CA2610724170
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102834670-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834670G>T , CM000672.2:g.102834670G>T GRCh38
NC_000010.10:g.104594427G>T , CM000672.1:g.104594427G>T GRCh37
NC_000010.9:g.104584417G>T NCBI36
NG_007955.1:g.7864C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.666+115C>A MANE Select ENSP00000358903.3:n.666+115C>A
ENST00000638190.1:c.666+115C>A ENSP00000492539.1:n.666+115C>A
ENST00000638272.1:c.298-1462C>A ENSP00000491508.1:n.298-1462C>A
ENST00000638971.1:c.666+115C>A ENSP00000492313.1:n.666+115C>A
ENST00000639393.1:c.666+115C>A ENSP00000492651.1:n.666+115C>A
ENST00000640633.1:n.428+115C>A
ENST00000369887.3:c.666+115C>A ENSP00000358903.3:n.666+115C>A
ENST00000489268.1:n.1035C>A
NM_000102.3:c.666+115C>A NP_000093.1:n.666+115C>A
NM_000102.4:c.666+115C>A MANE Select NP_000093.1:n.666+115C>A
Search 100 bp 5'
Search 100 bp 3'