Canonical Allele Identifier: CA2061986525
Gene: SART3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.108530192T= , CM000674.2:g.108530192T= GRCh38
NC_000012.11:g.108923969T= , CM000674.1:g.108923969T= GRCh37
NC_000012.10:g.107448099T= NCBI36
NG_012155.1:g.36197A=
NG_012155.2:g.36198A=

Transcript Alleles

HGVS Amino-acid change
ENST00000228284.8:c.1919A= ENSP00000228284.4:p.Lys640=
ENST00000546815.6:c.1865A= MANE Select ENSP00000449386.2:p.Lys622=
ENST00000651280.1:c.*1021A= ENSP00000498612.1:n.*1021A=
ENST00000228284.7:c.1865A= ENSP00000228284.3:p.Lys622=
ENST00000431469.6:c.1757A= ENSP00000414453.2:p.Lys586=
ENST00000546728.5:c.*759A= ENSP00000449743.1:n.*759A=
ENST00000546815.5:c.1919A= ENSP00000449386.1:p.Lys640=
NM_014706.3:c.1865A= NP_055521.1:p.Lys622=
XM_005269241.3:c.1919A= XP_005269298.1:p.Lys640=
XM_011539026.1:c.1001A= XP_011537328.1:p.Lys334=
NM_014706.4:c.1865A= MANE Select NP_055521.1:p.Lys622=
XM_005269241.5:c.1919A= XP_005269298.1:p.Lys640=
XM_024449284.1:c.1001A= XP_024305052.1:p.Lys334=