Canonical Allele Identifier: CA386436825

Gene: SART3

Linked Data

• MyVariant Identifiers: chr12:g.108923966C>G (hg19) ; chr12:g.108530189C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530189C>G , CM000674.2:g.108530189C>G	GRCh38
NC_000012.11:g.108923966C>G , CM000674.1:g.108923966C>G	GRCh37
NC_000012.10:g.107448096C>G	NCBI36
NG_012155.1:g.36200G>C
NG_012155.2:g.36201G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000228284.8:c.1922G>C	ENSP00000228284.4:p.Arg641Pro
ENST00000546815.6:c.1868G>C MANE Select	ENSP00000449386.2:p.Arg623Pro
ENST00000651280.1:c.*1024G>C	ENSP00000498612.1:n.*1024G>C
ENST00000228284.7:c.1868G>C	ENSP00000228284.3:p.Arg623Pro
ENST00000431469.6:c.1760G>C	ENSP00000414453.2:p.Arg587Pro
ENST00000546728.5:c.*762G>C	ENSP00000449743.1:n.*762G>C
ENST00000546815.5:c.1922G>C	ENSP00000449386.1:p.Arg641Pro
NM_014706.3:c.1868G>C	NP_055521.1:p.Arg623Pro
XM_005269241.3:c.1922G>C	XP_005269298.1:p.Arg641Pro
XM_011539026.1:c.1004G>C	XP_011537328.1:p.Arg335Pro
NM_014706.4:c.1868G>C MANE Select	NP_055521.1:p.Arg623Pro
XM_005269241.5:c.1922G>C	XP_005269298.1:p.Arg641Pro
XM_024449284.1:c.1004G>C	XP_024305052.1:p.Arg335Pro