Canonical Allele Identifier: CA2061986734

Gene: SART3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530338C= , CM000674.2:g.108530338C=	GRCh38
NC_000012.11:g.108924115C= , CM000674.1:g.108924115C=	GRCh37
NC_000012.10:g.107448245C=	NCBI36
NG_012155.1:g.36051G=
NG_012155.2:g.36052G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228284.8:c.1801-28G=	ENSP00000228284.4:n.1801-28G=
ENST00000546815.6:c.1747-28G= MANE Select	ENSP00000449386.2:n.1747-28G=
ENST00000651280.1:c.*903-28G=	ENSP00000498612.1:n.*903-28G=
ENST00000228284.7:c.1747-28G=	ENSP00000228284.3:n.1747-28G=
ENST00000431469.6:c.1639-28G=	ENSP00000414453.2:n.1639-28G=
ENST00000546728.5:c.*641-28G=	ENSP00000449743.1:n.*641-28G=
ENST00000546815.5:c.1801-28G=	ENSP00000449386.1:n.1801-28G=
ENST00000547528.5:c.*911-28G=	ENSP00000446577.1:n.*911-28G=
ENST00000548582.5:n.474-28G=
ENST00000619503.4:n.683-28G=
NM_014706.3:c.1747-28G=	NP_055521.1:n.1747-28G=
XM_005269241.3:c.1801-28G=	XP_005269298.1:n.1801-28G=
XM_011539026.1:c.883-28G=	XP_011537328.1:n.883-28G=
NM_014706.4:c.1747-28G= MANE Select	NP_055521.1:n.1747-28G=
XM_005269241.5:c.1801-28G=	XP_005269298.1:n.1801-28G=
XM_024449284.1:c.883-28G=	XP_024305052.1:n.883-28G=