Canonical Allele Identifier: CA2815621475

Gene: VSX1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.25077646A>C , CM000682.2:g.25077646A>C	GRCh38
NC_000020.10:g.25058282A>C , CM000682.1:g.25058282A>C	GRCh37
NC_000020.9:g.25006282A>C	NCBI36
NG_008101.1:g.9486T>G
NG_008101.2:g.9486T>G
NG_008101.3:g.9536T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376709.9:c.808+39T>G MANE Select	ENSP00000365899.3:n.808+39T>G
ENST00000376709.8:c.808+39T>G	ENSP00000365899.3:n.808+39T>G
ENST00000409285.6:c.808+39T>G	ENSP00000386612.2:n.808+39T>G
ENST00000409958.6:c.627+1183T>G	ENSP00000387069.2:n.627+1183T>G
ENST00000429762.7:c.808+39T>G	ENSP00000401690.3:n.808+39T>G
ENST00000444511.6:c.627+1183T>G	ENSP00000387720.2:n.627+1183T>G
ENST00000557285.1:n.315+39T>G
NM_001256271.1:c.627+1183T>G	NP_001243200.1:n.627+1183T>G
NM_001256272.1:c.808+39T>G	NP_001243201.1:n.808+39T>G
NM_014588.5:c.808+39T>G	NP_055403.2:n.808+39T>G
NR_045948.1:n.1091+39T>G
NR_045951.1:n.910+1183T>G
XM_017027837.1:c.808+39T>G	XP_016883326.1:n.808+39T>G
XM_017027838.1:c.627+1183T>G	XP_016883327.1:n.627+1183T>G
NM_014588.6:c.808+39T>G MANE Select	NP_055403.2:n.808+39T>G
NR_165181.1:n.818+39T>G
NR_165182.1:n.368+39T>G
NR_165183.1:n.368+39T>G
NR_165184.1:n.368+39T>G
NM_001256271.2:c.627+1183T>G	NP_001243200.1:n.627+1183T>G
NM_001256272.2:c.808+39T>G	NP_001243201.1:n.808+39T>G
NM_001378633.1:c.115+39T>G	NP_001365562.1:n.115+39T>G
NR_045948.2:n.853+39T>G
NR_045951.2:n.672+1183T>G
NR_165181.2:n.700+39T>G
NR_165182.2:n.368+39T>G
NR_165183.2:n.368+39T>G