Canonical Allele Identifier: CA412964015

Gene: CACNA1F

Linked Data

• MyVariant Identifiers: chrX:g.49072915C>A (hg19) ; chrX:g.49216455C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49216455C>A , CM000685.2:g.49216455C>A	GRCh38
NC_000023.10:g.49072915C>A , CM000685.1:g.49072915C>A	GRCh37
NC_000023.9:g.48959859C>A	NCBI36
NG_009095.2:g.21912G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.3163G>T MANE Select	ENSP00000321618.6:p.Asp1055Tyr
ENST00000323022.9:c.3163G>T	ENSP00000321618.5:p.Asp1055Tyr
ENST00000376251.5:c.3001G>T	ENSP00000365427.1:p.Asp1001Tyr
ENST00000376265.2:c.3196G>T	ENSP00000365441.2:p.Asp1066Tyr
NM_001256789.2:c.3163G>T	NP_001243718.1:p.Asp1055Tyr
NM_001256790.2:c.3001G>T	NP_001243719.1:p.Asp1001Tyr
NM_005183.3:c.3196G>T	NP_005174.2:p.Asp1066Tyr
XM_011543983.1:c.3001G>T	XP_011542285.1:p.Asp1001Tyr
XM_011543983.2:c.3001G>T	XP_011542285.1:p.Asp1001Tyr
XM_017029836.1:c.430G>T	XP_016885325.1:p.Asp144Tyr
NM_001256789.3:c.3163G>T MANE Select	NP_001243718.1:p.Asp1055Tyr
NM_001256790.3:c.3001G>T	NP_001243719.1:p.Asp1001Tyr
NM_005183.4:c.3196G>T	NP_005174.2:p.Asp1066Tyr