Canonical Allele Identifier: CA516377391

Gene: CACNA1F

Linked Data

• MyVariant Identifiers: chrX:g.49074252G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49217793G>C , CM000685.2:g.49217793G>C	GRCh38
NC_000023.10:g.49074252G>C , CM000685.1:g.49074252G>C	GRCh37
NC_000023.9:g.48961196G>C	NCBI36
NG_009095.2:g.20574C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.3051C>G MANE Select	ENSP00000321618.6:p.Thr1017=
ENST00000323022.9:c.3051C>G	ENSP00000321618.5:p.Thr1017=
ENST00000376251.5:c.2889C>G	ENSP00000365427.1:p.Thr963=
ENST00000376265.2:c.3084C>G	ENSP00000365441.2:p.Thr1028=
NM_001256789.2:c.3051C>G	NP_001243718.1:p.Thr1017=
NM_001256790.2:c.2889C>G	NP_001243719.1:p.Thr963=
NM_005183.3:c.3084C>G	NP_005174.2:p.Thr1028=
XM_011543983.1:c.2889C>G	XP_011542285.1:p.Thr963=
XM_011543983.2:c.2889C>G	XP_011542285.1:p.Thr963=
XM_017029836.1:c.318C>G	XP_016885325.1:p.Thr106=
NM_001256789.3:c.3051C>G MANE Select	NP_001243718.1:p.Thr1017=
NM_001256790.3:c.2889C>G	NP_001243719.1:p.Thr963=
NM_005183.4:c.3084C>G	NP_005174.2:p.Thr1028=