Canonical Allele Identifier: CA358783400

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178359983A>C (hg19) ; chr4:g.177438829A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438829A>C , CM000666.2:g.177438829A>C	GRCh38
NC_000004.11:g.178359983A>C , CM000666.1:g.178359983A>C	GRCh37
NC_000004.10:g.178596977A>C	NCBI36
NG_011845.2:g.8675T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.423T>G MANE Select	ENSP00000264595.2:p.Phe141Leu
ENST00000264595.6:c.423T>G	ENSP00000264595.2:p.Phe141Leu
ENST00000502310.5:c.78T>G	ENSP00000423798.1:p.Phe26Leu
ENST00000506853.5:n.457T>G
ENST00000510635.1:c.119T>G
ENST00000510955.5:n.344T>G
NM_000027.3:c.423T>G	NP_000018.2:p.Phe141Leu
NM_001171988.1:c.423T>G	NP_001165459.1:p.Phe141Leu
NR_033655.1:n.551T>G
XM_006714123.2:c.423T>G	XP_006714186.1:p.Phe141Leu
XR_001741155.2:n.517T>G
NM_000027.4:c.423T>G MANE Select	NP_000018.2:p.Phe141Leu
NM_001171988.2:c.423T>G	NP_001165459.1:p.Phe141Leu
NR_033655.2:n.485T>G