Canonical Allele Identifier: CA2396008643

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19724393G= , CM000684.2:g.19724393G=	GRCh38
NC_000022.10:g.19711916G= , CM000684.1:g.19711916G=	GRCh37
NC_000022.9:g.18091916G=	NCBI36
NG_007974.1:g.5851G= , LRG_478:g.5851G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.550G= (GP1BB) MANE Select	ENSP00000383382.2:p.Ala184=
ENST00000366425.3:c.550G= (GP1BB)	ENSP00000383382.2:p.Ala184=
ENST00000431044.5:c.*1635G= (SEPTIN5)	ENSP00000399685.1:n.*1635G=
NM_000407.4:c.550G= , LRG_478t1:c.550G= (GP1BB)	NP_000398.1:p.Ala184=
NR_037611.1:n.4290G=
NR_037612.1:n.2794G=
NM_000407.5:c.550G= (GP1BB) MANE Select	NP_000398.1:p.Ala184=