Canonical Allele Identifier: CA1515642197

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437665_177437666delinsTA , CM000666.2:g.177437665_177437666delinsTA	GRCh38
NC_000004.11:g.178358819_178358820delinsTA , CM000666.1:g.178358819_178358820delinsTA	GRCh37
NC_000004.10:g.178595813_178595814delinsTA	NCBI36
NG_011845.2:g.9838_9839delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.508-147_508-146delinsTA MANE Select	ENSP00000264595.2:n.508-147_508-146delinsTA
ENST00000264595.6:c.508-147_508-146delinsTA	ENSP00000264595.2:n.508-147_508-146delinsTA
ENST00000502310.5:c.163-147_163-146delinsTA	ENSP00000423798.1:n.163-147_163-146delinsTA
ENST00000506853.5:n.542-147_542-146delinsTA
ENST00000510635.1:c.204-147_204-146delinsTA
ENST00000510955.5:n.429-147_429-146delinsTA
NM_000027.3:c.508-147_508-146delinsTA	NP_000018.2:n.508-147_508-146delinsTA
NM_001171988.1:c.508-147_508-146delinsTA	NP_001165459.1:n.508-147_508-146delinsTA
NR_033655.1:n.636-147_636-146delinsTA
XM_006714123.2:c.508-147_508-146delinsTA	XP_006714186.1:n.508-147_508-146delinsTA
XR_001741155.2:n.602-147_602-146delinsTA
NM_000027.4:c.508-147_508-146delinsTA MANE Select	NP_000018.2:n.508-147_508-146delinsTA
NM_001171988.2:c.508-147_508-146delinsTA	NP_001165459.1:n.508-147_508-146delinsTA
NR_033655.2:n.570-147_570-146delinsTA