Canonical Allele Identifier: CA358783134

Gene: AGA

Linked Data

• gnomAD v4: 4-177438746-C-A
• MyVariant Identifiers: chr4:g.178359900C>A (hg19) ; chr4:g.177438746C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438746C>A , CM000666.2:g.177438746C>A	GRCh38
NC_000004.11:g.178359900C>A , CM000666.1:g.178359900C>A	GRCh37
NC_000004.10:g.178596894C>A	NCBI36
NG_011845.2:g.8758G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.506G>T MANE Select	ENSP00000264595.2:p.Arg169Met
ENST00000264595.6:c.506G>T	ENSP00000264595.2:p.Arg169Met
ENST00000502310.5:c.161G>T	ENSP00000423798.1:p.Arg54Met
ENST00000506853.5:n.540G>T
ENST00000510635.1:c.202G>T
ENST00000510955.5:n.427G>T
NM_000027.3:c.506G>T	NP_000018.2:p.Arg169Met
NM_001171988.1:c.506G>T	NP_001165459.1:p.Arg169Met
NR_033655.1:n.634G>T
XM_006714123.2:c.506G>T	XP_006714186.1:p.Arg169Met
XR_001741155.2:n.600G>T
NM_000027.4:c.506G>T MANE Select	NP_000018.2:p.Arg169Met
NM_001171988.2:c.506G>T	NP_001165459.1:p.Arg169Met
NR_033655.2:n.568G>T