Canonical Allele Identifier: CA5669568

Gene: CYP17A1

Linked Data

• dbSNP Id: rs770495392
• ExAC: 10:104594986 C / CCCCAGT
• gnomAD v2: 10-104594986-C-CCCCAGT
• gnomAD v4: 10-102835229-C-CCCCAGT
• MyVariant Identifiers: chr10:g.104594986_104594987insCCCAGT (hg19) ; chr10:g.102835229_102835230insCCCAGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835234_102835235insTCCCAG , CM000672.2:g.102835234_102835235insTCCCAG	GRCh38
NC_000010.10:g.104594991_104594992insTCCCAG , CM000672.1:g.104594991_104594992insTCCCAG	GRCh37
NC_000010.9:g.104584981_104584982insTCCCAG	NCBI36
NG_007955.1:g.7304_7305insACTGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.436+24_436+25insACTGGG MANE Select	ENSP00000358903.3:n.436+24_436+25insACTGG...
ENST00000638190.1:c.436+24_436+25insACTGGG	ENSP00000492539.1:n.436+24_436+25insACTGG...
ENST00000638272.1:c.297+1835_297+1836insACTGGG	ENSP00000491508.1:n.297+1835_297+1836insA...
ENST00000638971.1:c.436+24_436+25insACTGGG	ENSP00000492313.1:n.436+24_436+25insACTGG...
ENST00000639393.1:c.436+24_436+25insACTGGG	ENSP00000492651.1:n.436+24_436+25insACTGG...
ENST00000640633.1:n.198+24_198+25insACTGGG
ENST00000369887.3:c.436+24_436+25insACTGGG	ENSP00000358903.3:n.436+24_436+25insACTGG...
ENST00000489268.1:n.690+24_690+25insACTGGG
NM_000102.3:c.436+24_436+25insACTGGG	NP_000093.1:n.436+24_436+25insACTGGG
NM_000102.4:c.436+24_436+25insACTGGG MANE Select	NP_000093.1:n.436+24_436+25insACTGGG