Canonical Allele Identifier: CA481670140

Gene: SART3

Linked Data

• MyVariant Identifiers: chr12:g.108923974T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530197T>A , CM000674.2:g.108530197T>A	GRCh38
NC_000012.11:g.108923974T>A , CM000674.1:g.108923974T>A	GRCh37
NC_000012.10:g.107448104T>A	NCBI36
NG_012155.1:g.36192A>T
NG_012155.2:g.36193A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000228284.8:c.1914A>T	ENSP00000228284.4:p.Pro638=
ENST00000546815.6:c.1860A>T MANE Select	ENSP00000449386.2:p.Pro620=
ENST00000651280.1:c.*1016A>T	ENSP00000498612.1:n.*1016A>T
ENST00000228284.7:c.1860A>T	ENSP00000228284.3:p.Pro620=
ENST00000431469.6:c.1752A>T	ENSP00000414453.2:p.Pro584=
ENST00000546728.5:c.*754A>T	ENSP00000449743.1:n.*754A>T
ENST00000546815.5:c.1914A>T	ENSP00000449386.1:p.Pro638=
NM_014706.3:c.1860A>T	NP_055521.1:p.Pro620=
XM_005269241.3:c.1914A>T	XP_005269298.1:p.Pro638=
XM_011539026.1:c.996A>T	XP_011537328.1:p.Pro332=
NM_014706.4:c.1860A>T MANE Select	NP_055521.1:p.Pro620=
XM_005269241.5:c.1914A>T	XP_005269298.1:p.Pro638=
XM_024449284.1:c.996A>T	XP_024305052.1:p.Pro332=