Canonical Allele Identifier: CA1515644871

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439657G= , CM000666.2:g.177439657G=	GRCh38
NC_000004.11:g.178360811G= , CM000666.1:g.178360811G=	GRCh37
NC_000004.10:g.178597805G=	NCBI36
NG_011845.2:g.7847C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.313C= MANE Select	ENSP00000264595.2:p.Leu105=
ENST00000264595.6:c.313C=	ENSP00000264595.2:p.Leu105=
ENST00000506853.5:n.347C=
ENST00000510635.1:c.9C=
ENST00000510955.5:n.315+616C=
NM_000027.3:c.313C=	NP_000018.2:p.Leu105=
NM_001171988.1:c.313C=	NP_001165459.1:p.Leu105=
NR_033655.1:n.441C=
XM_006714123.2:c.313C=	XP_006714186.1:p.Leu105=
XR_001741155.2:n.407C=
NM_000027.4:c.313C= MANE Select	NP_000018.2:p.Leu105=
NM_001171988.2:c.313C=	NP_001165459.1:p.Leu105=
NR_033655.2:n.375C=