Canonical Allele Identifier: CA358785046

Gene: AGA

Linked Data

• gnomAD v4: 4-177442279-T-A
• MyVariant Identifiers: chr4:g.178363433T>A (hg19) ; chr4:g.177442279T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442279T>A , CM000666.2:g.177442279T>A	GRCh38
NC_000004.11:g.178363433T>A , CM000666.1:g.178363433T>A	GRCh37
NC_000004.10:g.178600427T>A	NCBI36
NG_011845.2:g.5225A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.97A>T MANE Select	ENSP00000264595.2:p.Thr33Ser
ENST00000264595.6:c.97A>T	ENSP00000264595.2:p.Thr33Ser
ENST00000506853.5:n.131A>T
ENST00000510955.5:n.131A>T
ENST00000511231.1:n.131A>T
NM_000027.3:c.97A>T	NP_000018.2:p.Thr33Ser
NM_001171988.1:c.97A>T	NP_001165459.1:p.Thr33Ser
NR_033655.1:n.225A>T
XM_006714123.2:c.97A>T	XP_006714186.1:p.Thr33Ser
XR_001741155.2:n.191A>T
NM_000027.4:c.97A>T MANE Select	NP_000018.2:p.Thr33Ser
NM_001171988.2:c.97A>T	NP_001165459.1:p.Thr33Ser
NR_033655.2:n.159A>T