Canonical Allele Identifier: CA386437574

Gene: SART3

Linked Data

• MyVariant Identifiers: chr12:g.108924089T>A (hg19) ; chr12:g.108530312T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530312T>A , CM000674.2:g.108530312T>A	GRCh38
NC_000012.11:g.108924089T>A , CM000674.1:g.108924089T>A	GRCh37
NC_000012.10:g.107448219T>A	NCBI36
NG_012155.1:g.36077A>T
NG_012155.2:g.36078A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228284.8:c.1801-2A>T	ENSP00000228284.4:n.1801-2A>T
ENST00000546815.6:c.1747-2A>T MANE Select	ENSP00000449386.2:n.1747-2A>T
ENST00000651280.1:c.*903-2A>T	ENSP00000498612.1:n.*903-2A>T
ENST00000228284.7:c.1747-2A>T	ENSP00000228284.3:n.1747-2A>T
ENST00000431469.6:c.1639-2A>T	ENSP00000414453.2:n.1639-2A>T
ENST00000546728.5:c.*641-2A>T	ENSP00000449743.1:n.*641-2A>T
ENST00000546815.5:c.1801-2A>T	ENSP00000449386.1:n.1801-2A>T
ENST00000547528.5:c.*911-2A>T	ENSP00000446577.1:n.*911-2A>T
ENST00000548582.5:n.474-2A>T
ENST00000619503.4:n.683-2A>T
NM_014706.3:c.1747-2A>T	NP_055521.1:n.1747-2A>T
XM_005269241.3:c.1801-2A>T	XP_005269298.1:n.1801-2A>T
XM_011539026.1:c.883-2A>T	XP_011537328.1:n.883-2A>T
NM_014706.4:c.1747-2A>T MANE Select	NP_055521.1:n.1747-2A>T
XM_005269241.5:c.1801-2A>T	XP_005269298.1:n.1801-2A>T
XM_024449284.1:c.883-2A>T	XP_024305052.1:n.883-2A>T