Canonical Allele Identifier: CA2739270362

Gene: AGA

Linked Data

• ClinVar Variation Id: 2855287
• ClinVar RCV Id: RCV003599829

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177434498G>A , CM000666.2:g.177434498G>A	GRCh38
NC_000004.11:g.178355652G>A , CM000666.1:g.178355652G>A	GRCh37
NC_000004.10:g.178592646G>A	NCBI36
NG_011845.2:g.13006C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.699-9C>T MANE Select	ENSP00000264595.2:n.699-9C>T
ENST00000264595.6:c.699-9C>T	ENSP00000264595.2:n.699-9C>T
ENST00000502310.5:c.278-17C>T	ENSP00000423798.1:n.278-17C>T
ENST00000506853.5:n.657-9C>T
ENST00000510635.1:c.373-17C>T
NM_000027.3:c.699-9C>T	NP_000018.2:n.699-9C>T
NM_001171988.1:c.677-17C>T	NP_001165459.1:n.677-17C>T
NR_033655.1:n.751-9C>T
XM_006714123.2:c.677-9C>T	XP_006714186.1:n.677-9C>T
XR_001741155.2:n.771-9C>T
NM_000027.4:c.699-9C>T MANE Select	NP_000018.2:n.699-9C>T
NM_001171988.2:c.677-17C>T	NP_001165459.1:n.677-17C>T
NR_033655.2:n.685-9C>T