Canonical Allele Identifier: CA789281925
Gene: C1QTNF7 HGNC NCBI
C1QTNF7-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1171664871
gnomAD v3: 4-15395650-G-C
gnomAD v4: 4-15395650-G-C
MyVariant Identifiers: chr4:g.15397274G>C (hg19) chr4:g.15395650G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15395650G>C , CM000666.2:g.15395650G>C GRCh38
NC_000004.11:g.15397274G>C , CM000666.1:g.15397274G>C GRCh37
NC_000004.10:g.15006372G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295297.4:c.14-40086G>C (C1QTNF7) ENSP00000295297.4:n.14-40086G>C
ENST00000382383.7:c.-9+20881G>C (C1QTNF7) ENSP00000371820.3:n.-9+20881G>C
ENST00000397700.6:c.14-40086G>C (C1QTNF7) ENSP00000380812.2:n.14-40086G>C
ENST00000429690.5:c.-9+20881G>C (C1QTNF7) ENSP00000410722.1:n.-9+20881G>C
NM_001135170.1:c.14-40086G>C (C1QTNF7) NP_001128642.1:n.14-40086G>C
NM_001135171.1:c.-9+20881G>C (C1QTNF7) NP_001128643.1:n.-9+20881G>C
NR_125911.1:n.86+32179C>G (C1QTNF7-AS1)
XM_011513772.1:c.14-40086G>C (C1QTNF7) XP_011512074.1:n.14-40086G>C
NM_001135170.2:c.14-40086G>C (C1QTNF7) NP_001128642.1:n.14-40086G>C
NM_001135171.2:c.-9+20881G>C (C1QTNF7) NP_001128643.1:n.-9+20881G>C
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