Canonical Allele Identifier: CA1876974377

Gene: RAB14

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121189639T= , CM000671.2:g.121189639T=	GRCh38
NC_000009.11:g.123951917T= , CM000671.1:g.123951917T=	GRCh37
NC_000009.10:g.122991738T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703996.1:c.284+915A=	ENSP00000515610.1:n.284+915A=
ENST00000703997.1:c.106+2532A=	ENSP00000515611.1:n.106+2532A=
ENST00000703998.1:c.227+915A=	ENSP00000515612.1:n.227+915A=
ENST00000703999.1:c.284+915A=	ENSP00000515613.1:n.284+915A=
ENST00000704000.1:c.284+915A=	ENSP00000515614.1:n.284+915A=
ENST00000704001.1:n.75-2620A=
ENST00000373840.9:c.284+915A= MANE Select	ENSP00000362946.4:n.284+915A=
ENST00000373840.8:c.284+915A=	ENSP00000362946.4:n.284+915A=
ENST00000451303.1:c.284+915A=	ENSP00000400107.1:n.284+915A=
NM_016322.3:c.284+915A=	NP_057406.2:n.284+915A=
NM_016322.4:c.284+915A= MANE Select	NP_057406.2:n.284+915A=