Canonical Allele Identifier: CA374943411

Gene: STXBP1 PTRH1

Linked Data

• MyVariant Identifiers: chr9:g.130453089G>A (hg19) ; chr9:g.127690810G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127690810G>A , CM000671.2:g.127690810G>A	GRCh38
NC_000009.11:g.130453089G>A , CM000671.1:g.130453089G>A	GRCh37
NC_000009.10:g.129492910G>A	NCBI36
NG_016623.1:g.83604G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000704680.1:c.1696G>A (STXBP1)	ENSP00000515991.1:p.Asp566Asn
ENST00000704681.1:c.1809G>A (STXBP1)	ENSP00000515992.1:n.1809G>A
ENST00000373299.5:c.1738G>A (STXBP1) MANE Select	ENSP00000362396.2:p.Asp580Asn
ENST00000373302.8:c.*52G>A (STXBP1) MANE Plus Clinical	ENSP00000362399.3:n.*52G>A
ENST00000626539.3:c.1696G>A (STXBP1)	ENSP00000487211.2:p.Asp566Asn
ENST00000635950.2:c.1703-4184G>A (STXBP1)	ENSP00000490903.1:n.1703-4184G>A
ENST00000636509.2:c.*693G>A (STXBP1)	ENSP00000490810.1:n.*693G>A
ENST00000636962.2:c.1703-4184G>A (STXBP1)	ENSP00000489762.1:n.1703-4184G>A
ENST00000637060.2:c.*1380G>A (STXBP1)	ENSP00000490674.2:n.*1380G>A
ENST00000637173.2:c.1696G>A (STXBP1)	ENSP00000490519.1:p.Asp566Asn
ENST00000637464.2:c.*2602G>A (STXBP1)	ENSP00000489655.2:n.*2602G>A
ENST00000637521.2:c.*52G>A (STXBP1)	ENSP00000489791.1:n.*52G>A
ENST00000637953.1:c.*84G>A (STXBP1)	ENSP00000490613.1:n.*84G>A
ENST00000641641.1:c.48C>T (PTRH1)	ENSP00000492921.1:p.Val16=
ENST00000650920.1:c.*52G>A (STXBP1)	ENSP00000498834.1:n.*52G>A
ENST00000373299.4:c.1738G>A (STXBP1)	ENSP00000362396.1:p.Asp580Asn
ENST00000373302.7:c.*52G>A (STXBP1)	ENSP00000362399.3:n.*52G>A
ENST00000626416.2:n.1574G>A (STXBP1)
ENST00000628638.1:n.330G>A (STXBP1)
ENST00000628768.1:n.677G>A (STXBP1)
NM_001032221.3:c.1738G>A (STXBP1)	NP_001027392.1:p.Asp580Asn
NM_003165.3:c.*52G>A (STXBP1)	NP_003156.1:n.*52G>A
NM_001032221.6:c.1738G>A (STXBP1) MANE Select	NP_001027392.1:p.Asp580Asn
NM_001374306.2:c.1729G>A (STXBP1)	NP_001361235.1:p.Asp577Asn
NM_001374307.2:c.*52G>A (STXBP1)	NP_001361236.1:n.*52G>A
NM_001374308.2:c.*52G>A (STXBP1)	NP_001361237.1:n.*52G>A
NM_001374309.2:c.1696G>A (STXBP1)	NP_001361238.1:p.Asp566Asn
NM_001374310.2:c.1696G>A (STXBP1)	NP_001361239.1:p.Asp566Asn
NM_001374311.2:c.1696G>A (STXBP1)	NP_001361240.1:p.Asp566Asn
NM_001374312.2:c.1696G>A (STXBP1)	NP_001361241.1:p.Asp566Asn
NM_001374313.2:c.*84G>A (STXBP1)	NP_001361242.1:n.*84G>A
NM_001374314.1:c.1703-4184G>A (STXBP1)	NP_001361243.1:n.1703-4184G>A
NM_001374315.2:c.*52G>A (STXBP1)	NP_001361244.1:n.*52G>A
NM_003165.6:c.*52G>A (STXBP1) MANE Plus Clinical	NP_003156.1:n.*52G>A