Canonical Allele Identifier: CA11873562
Gene: C1QTNF7 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1861046

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15396282G>A , CM000666.2:g.15396282G>A GRCh38
NC_000004.10:g.15007004G>A NCBI36
NC_000004.11:g.15397906G>A , CM000666.1:g.15397906G>A GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000295297.4:c.14-39454G>A ENSP00000295297.4:p.=
ENST00000382383.7:c.-9+21513G>A ENSP00000371820.3:p.=
ENST00000397700.6:c.14-39454G>A ENSP00000380812.2:p.=
ENST00000429690.5:c.-9+21513G>A ENSP00000410722.1:p.=
NM_001135170.1:c.14-39454G>A VV NP_001128642.1:p.=
NM_001135171.1:c.-9+21513G>A VV NP_001128643.1:p.=
NR_125911.1:n.86+31547C>T
XM_011513772.1:c.14-39454G>A XP_011512074.1:p.=