Canonical Allele Identifier: CA358782602

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178358580C>A (hg19) ; chr4:g.177437426C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437426C>A , CM000666.2:g.177437426C>A	GRCh38
NC_000004.11:g.178358580C>A , CM000666.1:g.178358580C>A	GRCh37
NC_000004.10:g.178595574C>A	NCBI36
NG_011845.2:g.10078G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.601G>T MANE Select	ENSP00000264595.2:p.Asp201Tyr
ENST00000264595.6:c.601G>T	ENSP00000264595.2:p.Asp201Tyr
ENST00000502310.5:c.256G>T	ENSP00000423798.1:p.Asp86Tyr
ENST00000506853.5:n.635G>T
ENST00000510635.1:c.297G>T
ENST00000510955.5:n.522G>T
NM_000027.3:c.601G>T	NP_000018.2:p.Asp201Tyr
NM_001171988.1:c.601G>T	NP_001165459.1:p.Asp201Tyr
NR_033655.1:n.729G>T
XM_006714123.2:c.601G>T	XP_006714186.1:p.Asp201Tyr
XR_001741155.2:n.695G>T
NM_000027.4:c.601G>T MANE Select	NP_000018.2:p.Asp201Tyr
NM_001171988.2:c.601G>T	NP_001165459.1:p.Asp201Tyr
NR_033655.2:n.663G>T