Canonical Allele Identifier: CA2061986673

Gene: SART3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530292C= , CM000674.2:g.108530292C=	GRCh38
NC_000012.11:g.108924069C= , CM000674.1:g.108924069C=	GRCh37
NC_000012.10:g.107448199C=	NCBI36
NG_012155.1:g.36097G=
NG_012155.2:g.36098G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000228284.8:c.1819G=	ENSP00000228284.4:p.Ala607=
ENST00000546815.6:c.1765G= MANE Select	ENSP00000449386.2:p.Ala589=
ENST00000651280.1:c.*921G=	ENSP00000498612.1:n.*921G=
ENST00000228284.7:c.1765G=	ENSP00000228284.3:p.Ala589=
ENST00000431469.6:c.1657G=	ENSP00000414453.2:p.Ala553=
ENST00000546728.5:c.*659G=	ENSP00000449743.1:n.*659G=
ENST00000546815.5:c.1819G=	ENSP00000449386.1:p.Ala607=
ENST00000547528.5:c.*929G=	ENSP00000446577.1:n.*929G=
ENST00000548582.5:n.492G=
ENST00000619503.4:n.701G=
NM_014706.3:c.1765G=	NP_055521.1:p.Ala589=
XM_005269241.3:c.1819G=	XP_005269298.1:p.Ala607=
XM_011539026.1:c.901G=	XP_011537328.1:p.Ala301=
NM_014706.4:c.1765G= MANE Select	NP_055521.1:p.Ala589=
XM_005269241.5:c.1819G=	XP_005269298.1:p.Ala607=
XM_024449284.1:c.901G=	XP_024305052.1:p.Ala301=