Canonical Allele Identifier: CA2428540158

Gene: CACNA1F

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49217726C= , CM000685.2:g.49217726C=	GRCh38
NC_000023.10:g.49074185C= , CM000685.1:g.49074185C=	GRCh37
NC_000023.9:g.48961129C=	NCBI36
NG_009095.2:g.20641G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000323022.10:c.3089+29G= MANE Select	ENSP00000321618.6:n.3089+29G=
ENST00000323022.9:c.3089+29G=	ENSP00000321618.5:n.3089+29G=
ENST00000376251.5:c.2927+29G=	ENSP00000365427.1:n.2927+29G=
ENST00000376265.2:c.3122+29G=	ENSP00000365441.2:n.3122+29G=
NM_001256789.2:c.3089+29G=	NP_001243718.1:n.3089+29G=
NM_001256790.2:c.2927+29G=	NP_001243719.1:n.2927+29G=
NM_005183.3:c.3122+29G=	NP_005174.2:n.3122+29G=
XM_011543983.1:c.2927+29G=	XP_011542285.1:n.2927+29G=
XM_011543983.2:c.2927+29G=	XP_011542285.1:n.2927+29G=
XM_017029836.1:c.356+29G=	XP_016885325.1:n.356+29G=
NM_001256789.3:c.3089+29G= MANE Select	NP_001243718.1:n.3089+29G=
NM_001256790.3:c.2927+29G=	NP_001243719.1:n.2927+29G=
NM_005183.4:c.3122+29G=	NP_005174.2:n.3122+29G=