Canonical Allele Identifier: CA442332828

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178360800A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439646A>G , CM000666.2:g.177439646A>G	GRCh38
NC_000004.11:g.178360800A>G , CM000666.1:g.178360800A>G	GRCh37
NC_000004.10:g.178597794A>G	NCBI36
NG_011845.2:g.7858T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.324T>C MANE Select	ENSP00000264595.2:p.Ile108=
ENST00000264595.6:c.324T>C	ENSP00000264595.2:p.Ile108=
ENST00000506853.5:n.358T>C
ENST00000510635.1:c.20T>C
ENST00000510955.5:n.315+627T>C
NM_000027.3:c.324T>C	NP_000018.2:p.Ile108=
NM_001171988.1:c.324T>C	NP_001165459.1:p.Ile108=
NR_033655.1:n.452T>C
XM_006714123.2:c.324T>C	XP_006714186.1:p.Ile108=
XR_001741155.2:n.418T>C
NM_000027.4:c.324T>C MANE Select	NP_000018.2:p.Ile108=
NM_001171988.2:c.324T>C	NP_001165459.1:p.Ile108=
NR_033655.2:n.386T>C