Canonical Allele Identifier: CA386436808

Gene: SART3

Linked Data

• MyVariant Identifiers: chr12:g.108923963C>A (hg19) ; chr12:g.108530186C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530186C>A , CM000674.2:g.108530186C>A	GRCh38
NC_000012.11:g.108923963C>A , CM000674.1:g.108923963C>A	GRCh37
NC_000012.10:g.107448093C>A	NCBI36
NG_012155.1:g.36203G>T
NG_012155.2:g.36204G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000228284.8:c.1925G>T	ENSP00000228284.4:p.Gly642Val
ENST00000546815.6:c.1871G>T MANE Select	ENSP00000449386.2:p.Gly624Val
ENST00000651280.1:c.*1027G>T	ENSP00000498612.1:n.*1027G>T
ENST00000228284.7:c.1871G>T	ENSP00000228284.3:p.Gly624Val
ENST00000431469.6:c.1763G>T	ENSP00000414453.2:p.Gly588Val
ENST00000546728.5:c.*765G>T	ENSP00000449743.1:n.*765G>T
ENST00000546815.5:c.1925G>T	ENSP00000449386.1:p.Gly642Val
NM_014706.3:c.1871G>T	NP_055521.1:p.Gly624Val
XM_005269241.3:c.1925G>T	XP_005269298.1:p.Gly642Val
XM_011539026.1:c.1007G>T	XP_011537328.1:p.Gly336Val
NM_014706.4:c.1871G>T MANE Select	NP_055521.1:p.Gly624Val
XM_005269241.5:c.1925G>T	XP_005269298.1:p.Gly642Val
XM_024449284.1:c.1007G>T	XP_024305052.1:p.Gly336Val