Canonical Allele Identifier: CA2759779293

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617974_186617975insTG , CM000665.2:g.186617974_186617975insTG	GRCh38
NC_000003.11:g.186335763_186335764insTG , CM000665.1:g.186335763_186335764insTG	GRCh37
NC_000003.10:g.187818457_187818458insTG	NCBI36
NG_011436.1:g.9914_9915insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-562_574-561insTG MANE Select	ENSP00000393887.2:n.574-562_574-561insTG
ENST00000273784.5:c.577-562_577-561insTG	ENSP00000273784.5:n.577-562_577-561insTG
ENST00000411641.6:c.574-562_574-561insTG	ENSP00000393887.2:n.574-562_574-561insTG
ENST00000478441.1:n.1254_1255insTG
NM_001622.2:c.574-562_574-561insTG	NP_001613.2:n.574-562_574-561insTG
NM_001354571.1:c.577-562_577-561insTG	NP_001341500.1:n.577-562_577-561insTG
NM_001354572.1:c.571-562_571-561insTG	NP_001341501.1:n.571-562_571-561insTG
NM_001354573.1:c.574-562_574-561insTG	NP_001341502.1:n.574-562_574-561insTG
NM_001622.3:c.574-562_574-561insTG	NP_001613.2:n.574-562_574-561insTG
NM_001622.4:c.574-562_574-561insTG MANE Select	NP_001613.2:n.574-562_574-561insTG
NM_001354571.2:c.577-562_577-561insTG	NP_001341500.1:n.577-562_577-561insTG
NM_001354572.2:c.571-562_571-561insTG	NP_001341501.1:n.571-562_571-561insTG
NM_001354573.2:c.574-562_574-561insTG	NP_001341502.1:n.574-562_574-561insTG