Canonical Allele Identifier: CA358782989

Gene: AGA

Linked Data

• gnomAD v4: 4-177437510-G-C
• MyVariant Identifiers: chr4:g.178358664G>C (hg19) ; chr4:g.177437510G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437510G>C , CM000666.2:g.177437510G>C	GRCh38
NC_000004.11:g.178358664G>C , CM000666.1:g.178358664G>C	GRCh37
NC_000004.10:g.178595658G>C	NCBI36
NG_011845.2:g.9994C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.517C>G MANE Select	ENSP00000264595.2:p.Pro173Ala
ENST00000264595.6:c.517C>G	ENSP00000264595.2:p.Pro173Ala
ENST00000502310.5:c.172C>G	ENSP00000423798.1:p.Pro58Ala
ENST00000506853.5:n.551C>G
ENST00000510635.1:c.213C>G
ENST00000510955.5:n.438C>G
NM_000027.3:c.517C>G	NP_000018.2:p.Pro173Ala
NM_001171988.1:c.517C>G	NP_001165459.1:p.Pro173Ala
NR_033655.1:n.645C>G
XM_006714123.2:c.517C>G	XP_006714186.1:p.Pro173Ala
XR_001741155.2:n.611C>G
NM_000027.4:c.517C>G MANE Select	NP_000018.2:p.Pro173Ala
NM_001171988.2:c.517C>G	NP_001165459.1:p.Pro173Ala
NR_033655.2:n.579C>G