Canonical Allele Identifier: CA358783288

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178359946G>T (hg19) ; chr4:g.177438792G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438792G>T , CM000666.2:g.177438792G>T	GRCh38
NC_000004.11:g.178359946G>T , CM000666.1:g.178359946G>T	GRCh37
NC_000004.10:g.178596940G>T	NCBI36
NG_011845.2:g.8712C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.460C>A MANE Select	ENSP00000264595.2:p.Leu154Ile
ENST00000264595.6:c.460C>A	ENSP00000264595.2:p.Leu154Ile
ENST00000502310.5:c.115C>A	ENSP00000423798.1:p.Leu39Ile
ENST00000506853.5:n.494C>A
ENST00000510635.1:c.156C>A
ENST00000510955.5:n.381C>A
NM_000027.3:c.460C>A	NP_000018.2:p.Leu154Ile
NM_001171988.1:c.460C>A	NP_001165459.1:p.Leu154Ile
NR_033655.1:n.588C>A
XM_006714123.2:c.460C>A	XP_006714186.1:p.Leu154Ile
XR_001741155.2:n.554C>A
NM_000027.4:c.460C>A MANE Select	NP_000018.2:p.Leu154Ile
NM_001171988.2:c.460C>A	NP_001165459.1:p.Leu154Ile
NR_033655.2:n.522C>A