Canonical Allele Identifier: CA169073440

Gene: AOC1

Linked Data

• dbSNP Id: rs34532106
• MyVariant Identifiers: chr7:g.150548902_150548903insG (hg19) ; chr7:g.150851814_150851815insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150851814_150851815insG , CM000669.2:g.150851814_150851815insG	GRCh38
NC_000007.13:g.150548902_150548903insG , CM000669.1:g.150548902_150548903insG	GRCh37
NC_000007.12:g.150179835_150179836insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467291.5:c.-92-301_-92-300insG	ENSP00000418328.1:n.-92-301_-92-300insG
ENST00000493429.5:c.-92-301_-92-300insG	ENSP00000418614.1:n.-92-301_-92-300insG
XM_011516008.1:c.-181-301_-181-300insG	XP_011514310.1:n.-181-301_-181-300insG
XM_011516009.1:c.-92-301_-92-300insG	XP_011514311.1:n.-92-301_-92-300insG
XR_928169.1:n.296-10370_296-10369insC
XR_928170.1:n.426-10370_426-10369insC
XR_928171.1:n.298-10370_298-10369insC
XM_017011944.1:c.-92-301_-92-300insG	XP_016867433.1:n.-92-301_-92-300insG
XM_017011945.1:c.-92-301_-92-300insG	XP_016867434.1:n.-92-301_-92-300insG
XR_928169.2:n.302-10370_302-10369insC
XR_928171.2:n.302-10370_302-10369insC