Canonical Allele Identifier: CA2061986665

Gene: SART3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530288A= , CM000674.2:g.108530288A=	GRCh38
NC_000012.11:g.108924065A= , CM000674.1:g.108924065A=	GRCh37
NC_000012.10:g.107448195A=	NCBI36
NG_012155.1:g.36101T=
NG_012155.2:g.36102T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000228284.8:c.1823T=	ENSP00000228284.4:p.Leu608=
ENST00000546815.6:c.1769T= MANE Select	ENSP00000449386.2:p.Leu590=
ENST00000651280.1:c.*925T=	ENSP00000498612.1:n.*925T=
ENST00000228284.7:c.1769T=	ENSP00000228284.3:p.Leu590=
ENST00000431469.6:c.1661T=	ENSP00000414453.2:p.Leu554=
ENST00000546728.5:c.*663T=	ENSP00000449743.1:n.*663T=
ENST00000546815.5:c.1823T=	ENSP00000449386.1:p.Leu608=
ENST00000547528.5:c.*933T=	ENSP00000446577.1:n.*933T=
ENST00000548582.5:n.496T=
ENST00000619503.4:n.705T=
NM_014706.3:c.1769T=	NP_055521.1:p.Leu590=
XM_005269241.3:c.1823T=	XP_005269298.1:p.Leu608=
XM_011539026.1:c.905T=	XP_011537328.1:p.Leu302=
NM_014706.4:c.1769T= MANE Select	NP_055521.1:p.Leu590=
XM_005269241.5:c.1823T=	XP_005269298.1:p.Leu608=
XM_024449284.1:c.905T=	XP_024305052.1:p.Leu302=