Canonical Allele Identifier: CA11873561

Gene: C1QTNF7 C1QTNF7-AS1

Linked Data

• dbSNP Id: rs1861045
• gnomAD v2: 4-15397871-T-C
• gnomAD v3: 4-15396247-T-C
• gnomAD v4: 4-15396247-T-C
• MyVariant Identifiers: chr4:g.15397871T>C (hg19) ; chr4:g.15396247T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15396247T>C , CM000666.2:g.15396247T>C	GRCh38
NC_000004.11:g.15397871T>C , CM000666.1:g.15397871T>C	GRCh37
NC_000004.10:g.15006969T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000295297.4:c.14-39489T>C (C1QTNF7)	ENSP00000295297.4:n.14-39489T>C
ENST00000382383.7:c.-9+21478T>C (C1QTNF7)	ENSP00000371820.3:n.-9+21478T>C
ENST00000397700.6:c.14-39489T>C (C1QTNF7)	ENSP00000380812.2:n.14-39489T>C
ENST00000429690.5:c.-9+21478T>C (C1QTNF7)	ENSP00000410722.1:n.-9+21478T>C
NM_001135170.1:c.14-39489T>C (C1QTNF7)	NP_001128642.1:n.14-39489T>C
NM_001135171.1:c.-9+21478T>C (C1QTNF7)	NP_001128643.1:n.-9+21478T>C
NR_125911.1:n.86+31582A>G (C1QTNF7-AS1)
XM_011513772.1:c.14-39489T>C (C1QTNF7)	XP_011512074.1:n.14-39489T>C
NM_001135170.2:c.14-39489T>C (C1QTNF7)	NP_001128642.1:n.14-39489T>C
NM_001135171.2:c.-9+21478T>C (C1QTNF7)	NP_001128643.1:n.-9+21478T>C