Canonical Allele Identifier: CA481670108

Gene: SART3

Linked Data

• MyVariant Identifiers: chr12:g.108923965G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530188G>C , CM000674.2:g.108530188G>C	GRCh38
NC_000012.11:g.108923965G>C , CM000674.1:g.108923965G>C	GRCh37
NC_000012.10:g.107448095G>C	NCBI36
NG_012155.1:g.36201C>G
NG_012155.2:g.36202C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000228284.8:c.1923C>G	ENSP00000228284.4:p.Arg641=
ENST00000546815.6:c.1869C>G MANE Select	ENSP00000449386.2:p.Arg623=
ENST00000651280.1:c.*1025C>G	ENSP00000498612.1:n.*1025C>G
ENST00000228284.7:c.1869C>G	ENSP00000228284.3:p.Arg623=
ENST00000431469.6:c.1761C>G	ENSP00000414453.2:p.Arg587=
ENST00000546728.5:c.*763C>G	ENSP00000449743.1:n.*763C>G
ENST00000546815.5:c.1923C>G	ENSP00000449386.1:p.Arg641=
NM_014706.3:c.1869C>G	NP_055521.1:p.Arg623=
XM_005269241.3:c.1923C>G	XP_005269298.1:p.Arg641=
XM_011539026.1:c.1005C>G	XP_011537328.1:p.Arg335=
NM_014706.4:c.1869C>G MANE Select	NP_055521.1:p.Arg623=
XM_005269241.5:c.1923C>G	XP_005269298.1:p.Arg641=
XM_024449284.1:c.1005C>G	XP_024305052.1:p.Arg335=