Canonical Allele Identifier: CA789282170

Gene: C1QTNF7 C1QTNF7-AS1

Linked Data

• dbSNP Id: rs1193465375
• gnomAD v3: 4-15396261-G-T
• gnomAD v4: 4-15396261-G-T
• MyVariant Identifiers: chr4:g.15397885G>T (hg19) ; chr4:g.15396261G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15396261G>T , CM000666.2:g.15396261G>T	GRCh38
NC_000004.11:g.15397885G>T , CM000666.1:g.15397885G>T	GRCh37
NC_000004.10:g.15006983G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000295297.4:c.14-39475G>T (C1QTNF7)	ENSP00000295297.4:n.14-39475G>T
ENST00000382383.7:c.-9+21492G>T (C1QTNF7)	ENSP00000371820.3:n.-9+21492G>T
ENST00000397700.6:c.14-39475G>T (C1QTNF7)	ENSP00000380812.2:n.14-39475G>T
ENST00000429690.5:c.-9+21492G>T (C1QTNF7)	ENSP00000410722.1:n.-9+21492G>T
NM_001135170.1:c.14-39475G>T (C1QTNF7)	NP_001128642.1:n.14-39475G>T
NM_001135171.1:c.-9+21492G>T (C1QTNF7)	NP_001128643.1:n.-9+21492G>T
NR_125911.1:n.86+31568C>A (C1QTNF7-AS1)
XM_011513772.1:c.14-39475G>T (C1QTNF7)	XP_011512074.1:n.14-39475G>T
NM_001135170.2:c.14-39475G>T (C1QTNF7)	NP_001128642.1:n.14-39475G>T
NM_001135171.2:c.-9+21492G>T (C1QTNF7)	NP_001128643.1:n.-9+21492G>T