Canonical Allele Identifier: CA442332554

Gene: AGA

Linked Data

• gnomAD v4: 4-177437409-A-G
• MyVariant Identifiers: chr4:g.178358563A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437409A>G , CM000666.2:g.177437409A>G	GRCh38
NC_000004.11:g.178358563A>G , CM000666.1:g.178358563A>G	GRCh37
NC_000004.10:g.178595557A>G	NCBI36
NG_011845.2:g.10095T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.618T>C MANE Select	ENSP00000264595.2:p.Thr206=
ENST00000264595.6:c.618T>C	ENSP00000264595.2:p.Thr206=
ENST00000502310.5:c.273T>C	ENSP00000423798.1:p.Thr91=
ENST00000506853.5:n.652T>C
ENST00000510635.1:c.314T>C
ENST00000510955.5:n.539T>C
NM_000027.3:c.618T>C	NP_000018.2:p.Thr206=
NM_001171988.1:c.618T>C	NP_001165459.1:p.Thr206=
NR_033655.1:n.746T>C
XM_006714123.2:c.618T>C	XP_006714186.1:p.Thr206=
XR_001741155.2:n.712T>C
NM_000027.4:c.618T>C MANE Select	NP_000018.2:p.Thr206=
NM_001171988.2:c.618T>C	NP_001165459.1:p.Thr206=
NR_033655.2:n.680T>C