Canonical Allele Identifier: CA358782862

Gene: AGA

Linked Data

• gnomAD v4: 4-177437481-G-C
• MyVariant Identifiers: chr4:g.178358635G>C (hg19) ; chr4:g.177437481G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437481G>C , CM000666.2:g.177437481G>C	GRCh38
NC_000004.11:g.178358635G>C , CM000666.1:g.178358635G>C	GRCh37
NC_000004.10:g.178595629G>C	NCBI36
NG_011845.2:g.10023C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.546C>G MANE Select	ENSP00000264595.2:p.Tyr182Ter
ENST00000264595.6:c.546C>G	ENSP00000264595.2:p.Tyr182Ter
ENST00000502310.5:c.201C>G	ENSP00000423798.1:p.Tyr67Ter
ENST00000506853.5:n.580C>G
ENST00000510635.1:c.242C>G
ENST00000510955.5:n.467C>G
NM_000027.3:c.546C>G	NP_000018.2:p.Tyr182Ter
NM_001171988.1:c.546C>G	NP_001165459.1:p.Tyr182Ter
NR_033655.1:n.674C>G
XM_006714123.2:c.546C>G	XP_006714186.1:p.Tyr182Ter
XR_001741155.2:n.640C>G
NM_000027.4:c.546C>G MANE Select	NP_000018.2:p.Tyr182Ter
NM_001171988.2:c.546C>G	NP_001165459.1:p.Tyr182Ter
NR_033655.2:n.608C>G