Canonical Allele Identifier: CA412964119

Gene: CACNA1F

Linked Data

• gnomAD v4: X-49216506-C-A
• MyVariant Identifiers: chrX:g.49072966C>A (hg19) ; chrX:g.49216506C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49216506C>A , CM000685.2:g.49216506C>A	GRCh38
NC_000023.10:g.49072966C>A , CM000685.1:g.49072966C>A	GRCh37
NC_000023.9:g.48959910C>A	NCBI36
NG_009095.2:g.21861G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.3112G>T MANE Select	ENSP00000321618.6:p.Asp1038Tyr
ENST00000323022.9:c.3112G>T	ENSP00000321618.5:p.Asp1038Tyr
ENST00000376251.5:c.2950G>T	ENSP00000365427.1:p.Asp984Tyr
ENST00000376265.2:c.3145G>T	ENSP00000365441.2:p.Asp1049Tyr
NM_001256789.2:c.3112G>T	NP_001243718.1:p.Asp1038Tyr
NM_001256790.2:c.2950G>T	NP_001243719.1:p.Asp984Tyr
NM_005183.3:c.3145G>T	NP_005174.2:p.Asp1049Tyr
XM_011543983.1:c.2950G>T	XP_011542285.1:p.Asp984Tyr
XM_011543983.2:c.2950G>T	XP_011542285.1:p.Asp984Tyr
XM_017029836.1:c.379G>T	XP_016885325.1:p.Asp127Tyr
NM_001256789.3:c.3112G>T MANE Select	NP_001243718.1:p.Asp1038Tyr
NM_001256790.3:c.2950G>T	NP_001243719.1:p.Asp984Tyr
NM_005183.4:c.3145G>T	NP_005174.2:p.Asp1049Tyr