Canonical Allele Identifier: CA386437443

Gene: SART3

Linked Data

• MyVariant Identifiers: chr12:g.108924068G>T (hg19) ; chr12:g.108530291G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530291G>T , CM000674.2:g.108530291G>T	GRCh38
NC_000012.11:g.108924068G>T , CM000674.1:g.108924068G>T	GRCh37
NC_000012.10:g.107448198G>T	NCBI36
NG_012155.1:g.36098C>A
NG_012155.2:g.36099C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000228284.8:c.1820C>A	ENSP00000228284.4:p.Ala607Asp
ENST00000546815.6:c.1766C>A MANE Select	ENSP00000449386.2:p.Ala589Asp
ENST00000651280.1:c.*922C>A	ENSP00000498612.1:n.*922C>A
ENST00000228284.7:c.1766C>A	ENSP00000228284.3:p.Ala589Asp
ENST00000431469.6:c.1658C>A	ENSP00000414453.2:p.Ala553Asp
ENST00000546728.5:c.*660C>A	ENSP00000449743.1:n.*660C>A
ENST00000546815.5:c.1820C>A	ENSP00000449386.1:p.Ala607Asp
ENST00000547528.5:c.*930C>A	ENSP00000446577.1:n.*930C>A
ENST00000548582.5:n.493C>A
ENST00000619503.4:n.702C>A
NM_014706.3:c.1766C>A	NP_055521.1:p.Ala589Asp
XM_005269241.3:c.1820C>A	XP_005269298.1:p.Ala607Asp
XM_011539026.1:c.902C>A	XP_011537328.1:p.Ala301Asp
NM_014706.4:c.1766C>A MANE Select	NP_055521.1:p.Ala589Asp
XM_005269241.5:c.1820C>A	XP_005269298.1:p.Ala607Asp
XM_024449284.1:c.902C>A	XP_024305052.1:p.Ala301Asp