Canonical Allele Identifier: CA2061986658

Gene: SART3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530286C= , CM000674.2:g.108530286C=	GRCh38
NC_000012.11:g.108924063C= , CM000674.1:g.108924063C=	GRCh37
NC_000012.10:g.107448193C=	NCBI36
NG_012155.1:g.36103G=
NG_012155.2:g.36104G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000228284.8:c.1825G=	ENSP00000228284.4:p.Val609=
ENST00000546815.6:c.1771G= MANE Select	ENSP00000449386.2:p.Val591=
ENST00000651280.1:c.*927G=	ENSP00000498612.1:n.*927G=
ENST00000228284.7:c.1771G=	ENSP00000228284.3:p.Val591=
ENST00000431469.6:c.1663G=	ENSP00000414453.2:p.Val555=
ENST00000546728.5:c.*665G=	ENSP00000449743.1:n.*665G=
ENST00000546815.5:c.1825G=	ENSP00000449386.1:p.Val609=
ENST00000547528.5:c.*935G=	ENSP00000446577.1:n.*935G=
ENST00000548582.5:n.498G=
ENST00000619503.4:n.707G=
NM_014706.3:c.1771G=	NP_055521.1:p.Val591=
XM_005269241.3:c.1825G=	XP_005269298.1:p.Val609=
XM_011539026.1:c.907G=	XP_011537328.1:p.Val303=
NM_014706.4:c.1771G= MANE Select	NP_055521.1:p.Val591=
XM_005269241.5:c.1825G=	XP_005269298.1:p.Val609=
XM_024449284.1:c.907G=	XP_024305052.1:p.Val303=