Canonical Allele Identifier: CA385037280

Gene: AAAS

Linked Data

• gnomAD v4: 12-53307690-G-A
• MyVariant Identifiers: chr12:g.53701474G>A (hg19) ; chr12:g.53307690G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307690G>A , CM000674.2:g.53307690G>A	GRCh38
NC_000012.11:g.53701474G>A , CM000674.1:g.53701474G>A	GRCh37
NC_000012.10:g.51987741G>A	NCBI36
NG_016775.1:g.18939C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1440C>T MANE Select	ENSP00000209873.4:p.Ala480=
ENST00000546562.6:n.2504C>T
ENST00000547238.6:n.2076C>T
ENST00000547520.6:n.1556C>T
ENST00000547757.2:c.*358C>T	ENSP00000448020.2:n.*358C>T
ENST00000548880.2:n.1890C>T
ENST00000548931.6:c.875C>T	ENSP00000457518.1:p.Pro292Leu
ENST00000549450.6:n.1374C>T
ENST00000552161.6:n.2518C>T
ENST00000672797.1:n.1929C>T
ENST00000209873.8:c.1440C>T	ENSP00000209873.4:p.Ala480=
ENST00000394384.7:c.1341C>T	ENSP00000377908.3:p.Ala447=
ENST00000548931.5:c.875C>T	ENSP00000457518.1:p.Pro292Leu
ENST00000550286.5:c.1068C>T	ENSP00000446885.1:p.Ala356=
ENST00000552876.5:n.1783C>T
NM_001173466.1:c.1341C>T	NP_001166937.1:p.Ala447=
NM_015665.5:c.1440C>T	NP_056480.1:p.Ala480=
XM_006719617.2:c.1455C>T	XP_006719680.1:p.Ala485=
XM_011538777.1:c.1497C>T	XP_011537079.1:p.Ala499=
XM_011538778.1:c.1482C>T	XP_011537080.1:p.Ala494=
XM_011538779.1:c.1398C>T	XP_011537081.1:p.Ala466=
XM_011538780.1:c.1383C>T	XP_011537082.1:p.Ala461=
XM_011538781.1:c.831C>T	XP_011537083.1:p.Ala277=
XM_011538778.2:c.1482C>T	XP_011537080.1:p.Ala494=
XM_011538780.2:c.1383C>T	XP_011537082.1:p.Ala461=
XR_001748875.2:n.1497C>T
NM_015665.6:c.1440C>T MANE Select	NP_056480.1:p.Ala480=
NM_001173466.2:c.1341C>T	NP_001166937.1:p.Ala447=