Canonical Allele Identifier: CA2759779120

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186614811_186614813del , CM000665.2:g.186614811_186614813del	GRCh38
NC_000003.11:g.186332600_186332602del , CM000665.1:g.186332600_186332602del	GRCh37
NC_000003.10:g.187815294_187815296del	NCBI36
NG_011436.1:g.6751_6753del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.214-874_214-872del MANE Select	ENSP00000393887.2:n.214-874_214-872del
ENST00000273784.5:c.214-874_214-872del	ENSP00000273784.5:n.214-874_214-872del
ENST00000411641.6:c.214-874_214-872del	ENSP00000393887.2:n.214-874_214-872del
ENST00000478441.1:n.271-874_271-872del
NM_001622.2:c.214-874_214-872del	NP_001613.2:n.214-874_214-872del
NM_001354571.1:c.214-874_214-872del	NP_001341500.1:n.214-874_214-872del
NM_001354572.1:c.214-877_214-875del	NP_001341501.1:n.214-877_214-875del
NM_001354573.1:c.214-874_214-872del	NP_001341502.1:n.214-874_214-872del
NM_001622.3:c.214-874_214-872del	NP_001613.2:n.214-874_214-872del
NM_001622.4:c.214-874_214-872del MANE Select	NP_001613.2:n.214-874_214-872del
NM_001354571.2:c.214-874_214-872del	NP_001341500.1:n.214-874_214-872del
NM_001354572.2:c.214-877_214-875del	NP_001341501.1:n.214-877_214-875del
NM_001354573.2:c.214-874_214-872del	NP_001341502.1:n.214-874_214-872del