Canonical Allele Identifier: CA2672747973

Gene: AGA

Linked Data

• gnomAD v4: 4-177439704-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439704A>G , CM000666.2:g.177439704A>G	GRCh38
NC_000004.11:g.178360858A>G , CM000666.1:g.178360858A>G	GRCh37
NC_000004.10:g.178597852A>G	NCBI36
NG_011845.2:g.7800T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.282-16T>C MANE Select	ENSP00000264595.2:n.282-16T>C
ENST00000264595.6:c.282-16T>C	ENSP00000264595.2:n.282-16T>C
ENST00000506853.5:n.316-16T>C
ENST00000510955.5:n.315+569T>C
NM_000027.3:c.282-16T>C	NP_000018.2:n.282-16T>C
NM_001171988.1:c.282-16T>C	NP_001165459.1:n.282-16T>C
NR_033655.1:n.410-16T>C
XM_006714123.2:c.282-16T>C	XP_006714186.1:n.282-16T>C
XR_001741155.2:n.376-16T>C
NM_000027.4:c.282-16T>C MANE Select	NP_000018.2:n.282-16T>C
NM_001171988.2:c.282-16T>C	NP_001165459.1:n.282-16T>C
NR_033655.2:n.344-16T>C