Canonical Allele Identifier: CA2625651072

Gene: VSX2

Linked Data

• gnomAD v4: 14-74259815-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74259815_74259816insA , CM000676.2:g.74259815_74259816insA	GRCh38
NC_000014.8:g.74726518_74726519insA , CM000676.1:g.74726518_74726519insA	GRCh37
NC_000014.7:g.73796271_73796272insA	NCBI36
NG_013092.1:g.25344_25345insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261980.3:c.760+33_760+34insA MANE Select	ENSP00000261980.2:n.760+33_760+34insA
ENST00000261980.2:c.760+33_760+34insA	ENSP00000261980.2:n.760+33_760+34insA
NM_182894.2:c.760+33_760+34insA	NP_878314.1:n.760+33_760+34insA
XM_011536719.1:c.760+33_760+34insA	XP_011535021.1:n.760+33_760+34insA
NM_182894.3:c.760+33_760+34insA MANE Select	NP_878314.1:n.760+33_760+34insA