Canonical Allele Identifier: CA2745107

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620903G>C , CM000665.2:g.186620903G>C	GRCh38
NC_000003.11:g.186338692G>C , CM000665.1:g.186338692G>C	GRCh37
NC_000003.10:g.187821386G>C	NCBI36
NG_011436.1:g.12843G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001622.4:c.1077G>C MANE Select	NP_001613.2:p.Pro359=
ENST00000411641.7:c.1077G>C MANE Select	ENSP00000393887.2:p.Pro359=
NM_001354571.1:c.1080G>C	NP_001341500.1:p.Pro360=
NM_001354571.2:c.1080G>C	NP_001341500.1:p.Pro360=
NM_001354572.1:c.1074G>C	NP_001341501.1:p.Pro358=
NM_001354572.2:c.1074G>C	NP_001341501.1:p.Pro358=
NM_001354573.1:c.993G>C	NP_001341502.1:p.Pro331=
NM_001354573.2:c.993G>C	NP_001341502.1:p.Pro331=
NM_001622.2:c.1077G>C	NP_001613.2:p.Pro359=
NM_001622.3:c.1077G>C	NP_001613.2:p.Pro359=
ENST00000273784.5:c.1080G>C	ENSP00000273784.5:p.Pro360=
ENST00000411641.6:c.1077G>C	ENSP00000393887.2:p.Pro359=