Canonical Allele Identifier: CA1515642174
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177437647_177437648delinsTA , CM000666.2:g.177437647_177437648delinsTA GRCh38
NC_000004.11:g.178358801_178358802delinsTA , CM000666.1:g.178358801_178358802delinsTA GRCh37
NC_000004.10:g.178595795_178595796delinsTA NCBI36
NG_011845.2:g.9856_9857delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.508-129_508-128delinsTA MANE Select ENSP00000264595.2:n.508-129_508-128delinsTA
ENST00000264595.6:c.508-129_508-128delinsTA ENSP00000264595.2:n.508-129_508-128delinsTA
ENST00000502310.5:c.163-129_163-128delinsTA ENSP00000423798.1:n.163-129_163-128delinsTA
ENST00000506853.5:n.542-129_542-128delinsTA
ENST00000510635.1:c.204-129_204-128delinsTA
ENST00000510955.5:n.429-129_429-128delinsTA
NM_000027.3:c.508-129_508-128delinsTA NP_000018.2:n.508-129_508-128delinsTA
NM_001171988.1:c.508-129_508-128delinsTA NP_001165459.1:n.508-129_508-128delinsTA
NR_033655.1:n.636-129_636-128delinsTA
XM_006714123.2:c.508-129_508-128delinsTA XP_006714186.1:n.508-129_508-128delinsTA
XR_001741155.2:n.602-129_602-128delinsTA
NM_000027.4:c.508-129_508-128delinsTA MANE Select NP_000018.2:n.508-129_508-128delinsTA
NM_001171988.2:c.508-129_508-128delinsTA NP_001165459.1:n.508-129_508-128delinsTA
NR_033655.2:n.570-129_570-128delinsTA