Canonical Allele Identifier: CA2531311661

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438971_33438973del , CM000682.2:g.33438971_33438973del	GRCh38
NC_000020.10:g.32026777_32026779del , CM000682.1:g.32026777_32026779del	GRCh37
NC_000020.9:g.31490438_31490440del	NCBI36
NG_011622.1:g.9922_9924del , LRG_332:g.9922_9924del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.366_368del MANE Select	ENSP00000217381.2:p.Ala123del
ENST00000217381.2:c.366_368del	ENSP00000217381.2:p.Ala123del
NM_003098.2:c.366_368del , LRG_332t1:c.366_368del	NP_003089.1:p.Ala123del
XM_005260517.1:c.366_368del	XP_005260574.1:p.Ala123del
XM_011529007.1:c.366_368del	XP_011527309.1:p.Ala123del
XM_011529008.1:c.366_368del	XP_011527310.1:p.Ala123del
XR_936612.1:n.599_601del
XM_024451971.1:c.39_41del	XP_024307739.1:p.Ala14del
NM_003098.3:c.366_368del MANE Select	NP_003089.1:p.Ala123del