Canonical Allele Identifier: CA2745105

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620902C>T , CM000665.2:g.186620902C>T	GRCh38
NC_000003.11:g.186338691C>T , CM000665.1:g.186338691C>T	GRCh37
NC_000003.10:g.187821385C>T	NCBI36
NG_011436.1:g.12842C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001622.4:c.1076C>T MANE Select	NP_001613.2:p.Pro359Leu
ENST00000411641.7:c.1076C>T MANE Select	ENSP00000393887.2:p.Pro359Leu
NM_001354571.1:c.1079C>T	NP_001341500.1:p.Pro360Leu
NM_001354571.2:c.1079C>T	NP_001341500.1:p.Pro360Leu
NM_001354572.1:c.1073C>T	NP_001341501.1:p.Pro358Leu
NM_001354572.2:c.1073C>T	NP_001341501.1:p.Pro358Leu
NM_001354573.1:c.992C>T	NP_001341502.1:p.Pro331Leu
NM_001354573.2:c.992C>T	NP_001341502.1:p.Pro331Leu
NM_001622.2:c.1076C>T	NP_001613.2:p.Pro359Leu
NM_001622.3:c.1076C>T	NP_001613.2:p.Pro359Leu
ENST00000273784.5:c.1079C>T	ENSP00000273784.5:p.Pro360Leu
ENST00000411641.6:c.1076C>T	ENSP00000393887.2:p.Pro359Leu