Canonical Allele Identifier: CA1427018415
Gene: AHSG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186617914_186617915delinsAC , CM000665.2:g.186617914_186617915delinsAC GRCh38
NC_000003.11:g.186335703_186335704delinsAC , CM000665.1:g.186335703_186335704delinsAC GRCh37
NC_000003.10:g.187818397_187818398delinsAC NCBI36
NG_011436.1:g.9854_9855delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000411641.7:c.573+564_573+565delinsAC MANE Select ENSP00000393887.2:n.573+564_573+565delinsAC
ENST00000273784.5:c.576+564_576+565delinsAC ENSP00000273784.5:n.576+564_576+565delinsAC
ENST00000411641.6:c.573+564_573+565delinsAC ENSP00000393887.2:n.573+564_573+565delinsAC
ENST00000478441.1:n.1194_1195delinsAC
NM_001622.2:c.573+564_573+565delinsAC NP_001613.2:n.573+564_573+565delinsAC
NM_001354571.1:c.576+564_576+565delinsAC NP_001341500.1:n.576+564_576+565delinsAC
NM_001354572.1:c.570+564_570+565delinsAC NP_001341501.1:n.570+564_570+565delinsAC
NM_001354573.1:c.573+564_573+565delinsAC NP_001341502.1:n.573+564_573+565delinsAC
NM_001622.3:c.573+564_573+565delinsAC NP_001613.2:n.573+564_573+565delinsAC
NM_001622.4:c.573+564_573+565delinsAC MANE Select NP_001613.2:n.573+564_573+565delinsAC
NM_001354571.2:c.576+564_576+565delinsAC NP_001341500.1:n.576+564_576+565delinsAC
NM_001354572.2:c.570+564_570+565delinsAC NP_001341501.1:n.570+564_570+565delinsAC
NM_001354573.2:c.573+564_573+565delinsAC NP_001341502.1:n.573+564_573+565delinsAC