Canonical Allele Identifier: CA2620715772

Gene: SART3

Linked Data

• gnomAD v4: 12-108530197-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530200del , CM000674.2:g.108530200del	GRCh38
NC_000012.11:g.108923977del , CM000674.1:g.108923977del	GRCh37
NC_000012.10:g.107448107del	NCBI36
NG_012155.1:g.36191del
NG_012155.2:g.36192del

Transcript Alleles

HGVS	Amino-acid change
ENST00000228284.8:c.1913del	ENSP00000228284.4:p.Pro638GlnfsTer?
ENST00000546815.6:c.1859del MANE Select	ENSP00000449386.2:p.Pro620GlnfsTer?
ENST00000651280.1:c.*1015del	ENSP00000498612.1:n.*1015del
ENST00000228284.7:c.1859del	ENSP00000228284.3:p.Pro620GlnfsTer?
ENST00000431469.6:c.1751del	ENSP00000414453.2:p.Pro584GlnfsTer?
ENST00000546728.5:c.*753del	ENSP00000449743.1:n.*753del
ENST00000546815.5:c.1913del	ENSP00000449386.1:p.Pro638GlnfsTer?
NM_014706.3:c.1859del	NP_055521.1:p.Pro620GlnfsTer?
XM_005269241.3:c.1913del	XP_005269298.1:p.Pro638GlnfsTer?
XM_011539026.1:c.995del	XP_011537328.1:p.Pro332GlnfsTer?
NM_014706.4:c.1859del MANE Select	NP_055521.1:p.Pro620GlnfsTer?
XM_005269241.5:c.1913del	XP_005269298.1:p.Pro638GlnfsTer?
XM_024449284.1:c.995del	XP_024305052.1:p.Pro332GlnfsTer?