Canonical Allele Identifier: CA481670533

Gene: SART3

Linked Data

• dbSNP Id: rs543774350
• MyVariant Identifiers: chr12:g.108924070T>A (hg19) ; chr12:g.108530293T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530293T>A , CM000674.2:g.108530293T>A	GRCh38
NC_000012.11:g.108924070T>A , CM000674.1:g.108924070T>A	GRCh37
NC_000012.10:g.107448200T>A	NCBI36
NG_012155.1:g.36096A>T
NG_012155.2:g.36097A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000228284.8:c.1818A>T	ENSP00000228284.4:p.Ala606=
ENST00000546815.6:c.1764A>T MANE Select	ENSP00000449386.2:p.Ala588=
ENST00000651280.1:c.*920A>T	ENSP00000498612.1:n.*920A>T
ENST00000228284.7:c.1764A>T	ENSP00000228284.3:p.Ala588=
ENST00000431469.6:c.1656A>T	ENSP00000414453.2:p.Ala552=
ENST00000546728.5:c.*658A>T	ENSP00000449743.1:n.*658A>T
ENST00000546815.5:c.1818A>T	ENSP00000449386.1:p.Ala606=
ENST00000547528.5:c.*928A>T	ENSP00000446577.1:n.*928A>T
ENST00000548582.5:n.491A>T
ENST00000619503.4:n.700A>T
NM_014706.3:c.1764A>T	NP_055521.1:p.Ala588=
XM_005269241.3:c.1818A>T	XP_005269298.1:p.Ala606=
XM_011539026.1:c.900A>T	XP_011537328.1:p.Ala300=
NM_014706.4:c.1764A>T MANE Select	NP_055521.1:p.Ala588=
XM_005269241.5:c.1818A>T	XP_005269298.1:p.Ala606=
XM_024449284.1:c.900A>T	XP_024305052.1:p.Ala300=