Canonical Allele Identifier: CA2764653739
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177437321A>C , CM000666.2:g.177437321A>C GRCh38
NC_000004.11:g.178358475A>C , CM000666.1:g.178358475A>C GRCh37
NC_000004.10:g.178595469A>C NCBI36
NG_011845.2:g.10183T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.622+84T>G MANE Select ENSP00000264595.2:n.622+84T>G
ENST00000264595.6:c.622+84T>G ENSP00000264595.2:n.622+84T>G
ENST00000502310.5:c.277+84T>G ENSP00000423798.1:n.277+84T>G
ENST00000506853.5:n.656+84T>G
ENST00000510635.1:c.318+84T>G
ENST00000510955.5:n.627T>G
NM_000027.3:c.622+84T>G NP_000018.2:n.622+84T>G
NM_001171988.1:c.622+84T>G NP_001165459.1:n.622+84T>G
NR_033655.1:n.750+84T>G
XM_006714123.2:c.622+84T>G XP_006714186.1:n.622+84T>G
XR_001741155.2:n.716+84T>G
NM_000027.4:c.622+84T>G MANE Select NP_000018.2:n.622+84T>G
NM_001171988.2:c.622+84T>G NP_001165459.1:n.622+84T>G
NR_033655.2:n.684+84T>G