Canonical Allele Identifier: CA442332635

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178359911T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438757T>C , CM000666.2:g.177438757T>C	GRCh38
NC_000004.11:g.178359911T>C , CM000666.1:g.178359911T>C	GRCh37
NC_000004.10:g.178596905T>C	NCBI36
NG_011845.2:g.8747A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.495A>G MANE Select	ENSP00000264595.2:p.Pro165=
ENST00000264595.6:c.495A>G	ENSP00000264595.2:p.Pro165=
ENST00000502310.5:c.150A>G	ENSP00000423798.1:p.Pro50=
ENST00000506853.5:n.529A>G
ENST00000510635.1:c.191A>G
ENST00000510955.5:n.416A>G
NM_000027.3:c.495A>G	NP_000018.2:p.Pro165=
NM_001171988.1:c.495A>G	NP_001165459.1:p.Pro165=
NR_033655.1:n.623A>G
XM_006714123.2:c.495A>G	XP_006714186.1:p.Pro165=
XR_001741155.2:n.589A>G
NM_000027.4:c.495A>G MANE Select	NP_000018.2:p.Pro165=
NM_001171988.2:c.495A>G	NP_001165459.1:p.Pro165=
NR_033655.2:n.557A>G