Canonical Allele Identifier: CA516377314

Gene: CACNA1F

Linked Data

• MyVariant Identifiers: chrX:g.49072919G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49216459G>A , CM000685.2:g.49216459G>A	GRCh38
NC_000023.10:g.49072919G>A , CM000685.1:g.49072919G>A	GRCh37
NC_000023.9:g.48959863G>A	NCBI36
NG_009095.2:g.21908C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.3159C>T MANE Select	ENSP00000321618.6:p.Asn1053=
ENST00000323022.9:c.3159C>T	ENSP00000321618.5:p.Asn1053=
ENST00000376251.5:c.2997C>T	ENSP00000365427.1:p.Asn999=
ENST00000376265.2:c.3192C>T	ENSP00000365441.2:p.Asn1064=
NM_001256789.2:c.3159C>T	NP_001243718.1:p.Asn1053=
NM_001256790.2:c.2997C>T	NP_001243719.1:p.Asn999=
NM_005183.3:c.3192C>T	NP_005174.2:p.Asn1064=
XM_011543983.1:c.2997C>T	XP_011542285.1:p.Asn999=
XM_011543983.2:c.2997C>T	XP_011542285.1:p.Asn999=
XM_017029836.1:c.426C>T	XP_016885325.1:p.Asn142=
NM_001256789.3:c.3159C>T MANE Select	NP_001243718.1:p.Asn1053=
NM_001256790.3:c.2997C>T	NP_001243719.1:p.Asn999=
NM_005183.4:c.3192C>T	NP_005174.2:p.Asn1064=