Canonical Allele Identifier: CA358783477

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178360000C>A (hg19) ; chr4:g.177438846C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438846C>A , CM000666.2:g.177438846C>A	GRCh38
NC_000004.11:g.178360000C>A , CM000666.1:g.178360000C>A	GRCh37
NC_000004.10:g.178596994C>A	NCBI36
NG_011845.2:g.8658G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.406G>T MANE Select	ENSP00000264595.2:p.Ala136Ser
ENST00000264595.6:c.406G>T	ENSP00000264595.2:p.Ala136Ser
ENST00000502310.5:c.61G>T	ENSP00000423798.1:p.Ala21Ser
ENST00000506853.5:n.440G>T
ENST00000510635.1:c.102G>T
ENST00000510955.5:n.327G>T
NM_000027.3:c.406G>T	NP_000018.2:p.Ala136Ser
NM_001171988.1:c.406G>T	NP_001165459.1:p.Ala136Ser
NR_033655.1:n.534G>T
XM_006714123.2:c.406G>T	XP_006714186.1:p.Ala136Ser
XR_001741155.2:n.500G>T
NM_000027.4:c.406G>T MANE Select	NP_000018.2:p.Ala136Ser
NM_001171988.2:c.406G>T	NP_001165459.1:p.Ala136Ser
NR_033655.2:n.468G>T