Canonical Allele Identifier: CA358782725

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178358605A>C (hg19) ; chr4:g.177437451A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437451A>C , CM000666.2:g.177437451A>C	GRCh38
NC_000004.11:g.178358605A>C , CM000666.1:g.178358605A>C	GRCh37
NC_000004.10:g.178595599A>C	NCBI36
NG_011845.2:g.10053T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.576T>G MANE Select	ENSP00000264595.2:p.Ile192Met
ENST00000264595.6:c.576T>G	ENSP00000264595.2:p.Ile192Met
ENST00000502310.5:c.231T>G	ENSP00000423798.1:p.Ile77Met
ENST00000506853.5:n.610T>G
ENST00000510635.1:c.272T>G
ENST00000510955.5:n.497T>G
NM_000027.3:c.576T>G	NP_000018.2:p.Ile192Met
NM_001171988.1:c.576T>G	NP_001165459.1:p.Ile192Met
NR_033655.1:n.704T>G
XM_006714123.2:c.576T>G	XP_006714186.1:p.Ile192Met
XR_001741155.2:n.670T>G
NM_000027.4:c.576T>G MANE Select	NP_000018.2:p.Ile192Met
NM_001171988.2:c.576T>G	NP_001165459.1:p.Ile192Met
NR_033655.2:n.638T>G