Canonical Allele Identifier: CA386437467

Gene: SART3

Linked Data

• MyVariant Identifiers: chr12:g.108924072C>A (hg19) ; chr12:g.108530295C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530295C>A , CM000674.2:g.108530295C>A	GRCh38
NC_000012.11:g.108924072C>A , CM000674.1:g.108924072C>A	GRCh37
NC_000012.10:g.107448202C>A	NCBI36
NG_012155.1:g.36094G>T
NG_012155.2:g.36095G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000228284.8:c.1816G>T	ENSP00000228284.4:p.Ala606Ser
ENST00000546815.6:c.1762G>T MANE Select	ENSP00000449386.2:p.Ala588Ser
ENST00000651280.1:c.*918G>T	ENSP00000498612.1:n.*918G>T
ENST00000228284.7:c.1762G>T	ENSP00000228284.3:p.Ala588Ser
ENST00000431469.6:c.1654G>T	ENSP00000414453.2:p.Ala552Ser
ENST00000546728.5:c.*656G>T	ENSP00000449743.1:n.*656G>T
ENST00000546815.5:c.1816G>T	ENSP00000449386.1:p.Ala606Ser
ENST00000547528.5:c.*926G>T	ENSP00000446577.1:n.*926G>T
ENST00000548582.5:n.489G>T
ENST00000619503.4:n.698G>T
NM_014706.3:c.1762G>T	NP_055521.1:p.Ala588Ser
XM_005269241.3:c.1816G>T	XP_005269298.1:p.Ala606Ser
XM_011539026.1:c.898G>T	XP_011537328.1:p.Ala300Ser
NM_014706.4:c.1762G>T MANE Select	NP_055521.1:p.Ala588Ser
XM_005269241.5:c.1816G>T	XP_005269298.1:p.Ala606Ser
XM_024449284.1:c.898G>T	XP_024305052.1:p.Ala300Ser