Canonical Allele Identifier: CA2061986532
Gene: SART3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.108530198G= , CM000674.2:g.108530198G= GRCh38
NC_000012.11:g.108923975G= , CM000674.1:g.108923975G= GRCh37
NC_000012.10:g.107448105G= NCBI36
NG_012155.1:g.36191C=
NG_012155.2:g.36192C=

Transcript Alleles

HGVS Amino-acid change
ENST00000228284.8:c.1913C= ENSP00000228284.4:p.Pro638=
ENST00000546815.6:c.1859C= MANE Select ENSP00000449386.2:p.Pro620=
ENST00000651280.1:c.*1015C= ENSP00000498612.1:n.*1015C=
ENST00000228284.7:c.1859C= ENSP00000228284.3:p.Pro620=
ENST00000431469.6:c.1751C= ENSP00000414453.2:p.Pro584=
ENST00000546728.5:c.*753C= ENSP00000449743.1:n.*753C=
ENST00000546815.5:c.1913C= ENSP00000449386.1:p.Pro638=
NM_014706.3:c.1859C= NP_055521.1:p.Pro620=
XM_005269241.3:c.1913C= XP_005269298.1:p.Pro638=
XM_011539026.1:c.995C= XP_011537328.1:p.Pro332=
NM_014706.4:c.1859C= MANE Select NP_055521.1:p.Pro620=
XM_005269241.5:c.1913C= XP_005269298.1:p.Pro638=
XM_024449284.1:c.995C= XP_024305052.1:p.Pro332=