Canonical Allele Identifier: CA2764653748

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437617_177437618insCACCC , CM000666.2:g.177437617_177437618insCACCC	GRCh38
NC_000004.11:g.178358771_178358772insCACCC , CM000666.1:g.178358771_178358772insCACCC	GRCh37
NC_000004.10:g.178595765_178595766insCACCC	NCBI36
NG_011845.2:g.9886_9887insGGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.508-99_508-98insGGGTG MANE Select	ENSP00000264595.2:n.508-99_508-98insGGGTG
ENST00000264595.6:c.508-99_508-98insGGGTG	ENSP00000264595.2:n.508-99_508-98insGGGTG
ENST00000502310.5:c.163-99_163-98insGGGTG	ENSP00000423798.1:n.163-99_163-98insGGGTG
ENST00000506853.5:n.542-99_542-98insGGGTG
ENST00000510635.1:c.204-99_204-98insGGGTG
ENST00000510955.5:n.429-99_429-98insGGGTG
NM_000027.3:c.508-99_508-98insGGGTG	NP_000018.2:n.508-99_508-98insGGGTG
NM_001171988.1:c.508-99_508-98insGGGTG	NP_001165459.1:n.508-99_508-98insGGGTG
NR_033655.1:n.636-99_636-98insGGGTG
XM_006714123.2:c.508-99_508-98insGGGTG	XP_006714186.1:n.508-99_508-98insGGGTG
XR_001741155.2:n.602-99_602-98insGGGTG
NM_000027.4:c.508-99_508-98insGGGTG MANE Select	NP_000018.2:n.508-99_508-98insGGGTG
NM_001171988.2:c.508-99_508-98insGGGTG	NP_001165459.1:n.508-99_508-98insGGGTG
NR_033655.2:n.570-99_570-98insGGGTG