Canonical Allele Identifier: CA516377438

Gene: CACNA1F

Linked Data

• dbSNP Id: rs1557107823
• gnomAD v3: X-49217961-G-A
• gnomAD v4: X-49217961-G-A
• MyVariant Identifiers: chrX:g.49074420G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49217961G>A , CM000685.2:g.49217961G>A	GRCh38
NC_000023.10:g.49074420G>A , CM000685.1:g.49074420G>A	GRCh37
NC_000023.9:g.48961364G>A	NCBI36
NG_009095.2:g.20406C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.2973C>T MANE Select	ENSP00000321618.6:p.Asn991=
ENST00000323022.9:c.2973C>T	ENSP00000321618.5:p.Asn991=
ENST00000376251.5:c.2811C>T	ENSP00000365427.1:p.Asn937=
ENST00000376265.2:c.3006C>T	ENSP00000365441.2:p.Asn1002=
NM_001256789.2:c.2973C>T	NP_001243718.1:p.Asn991=
NM_001256790.2:c.2811C>T	NP_001243719.1:p.Asn937=
NM_005183.3:c.3006C>T	NP_005174.2:p.Asn1002=
XM_011543983.1:c.2811C>T	XP_011542285.1:p.Asn937=
XM_011543983.2:c.2811C>T	XP_011542285.1:p.Asn937=
XM_017029836.1:c.240C>T	XP_016885325.1:p.Asn80=
NM_001256789.3:c.2973C>T MANE Select	NP_001243718.1:p.Asn991=
NM_001256790.3:c.2811C>T	NP_001243719.1:p.Asn937=
NM_005183.4:c.3006C>T	NP_005174.2:p.Asn1002=