Canonical Allele Identifier: CA358782358

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178355641C>A (hg19) ; chr4:g.177434487C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177434487C>A , CM000666.2:g.177434487C>A	GRCh38
NC_000004.11:g.178355641C>A , CM000666.1:g.178355641C>A	GRCh37
NC_000004.10:g.178592635C>A	NCBI36
NG_011845.2:g.13017G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.701G>T MANE Select	ENSP00000264595.2:p.Arg234Leu
ENST00000264595.6:c.701G>T	ENSP00000264595.2:p.Arg234Leu
ENST00000502310.5:c.278-6G>T	ENSP00000423798.1:n.278-6G>T
ENST00000506853.5:n.659G>T
ENST00000510635.1:c.373-6G>T
NM_000027.3:c.701G>T	NP_000018.2:p.Arg234Leu
NM_001171988.1:c.677-6G>T	NP_001165459.1:n.677-6G>T
NR_033655.1:n.753G>T
XM_006714123.2:c.679G>T	XP_006714186.1:p.Val227Leu
XR_001741155.2:n.773G>T
NM_000027.4:c.701G>T MANE Select	NP_000018.2:p.Arg234Leu
NM_001171988.2:c.677-6G>T	NP_001165459.1:n.677-6G>T
NR_033655.2:n.687G>T