Canonical Allele Identifier: CA411432233

Gene: C1QTNF6

Linked Data

• gnomAD v3: 22-37185352-A-G
• gnomAD v4: 22-37185352-A-G
• MyVariant Identifiers: chr22:g.37581392A>G (hg19) ; chr22:g.37185352A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37185352A>G , CM000684.2:g.37185352A>G	GRCh38
NC_000022.10:g.37581392A>G , CM000684.1:g.37581392A>G	GRCh37
NC_000022.9:g.35911338A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337843.7:c.155T>C MANE Select	ENSP00000338812.2:p.Val52Ala
ENST00000337843.6:c.155T>C	ENSP00000338812.2:p.Val52Ala
ENST00000397110.6:c.155T>C	ENSP00000380299.2:p.Val52Ala
ENST00000434784.1:c.155T>C	ENSP00000399243.1:p.Val52Ala
ENST00000470655.5:n.3645T>C
ENST00000493023.1:n.597T>C
NM_031910.3:c.155T>C	NP_114116.3:p.Val52Ala
NM_182486.1:c.155T>C	NP_872292.1:p.Val52Ala
XM_006724125.2:c.98T>C	XP_006724188.1:p.Val33Ala
XM_011529857.1:c.98T>C	XP_011528159.1:p.Val33Ala
NM_001365878.1:c.98T>C	NP_001352807.1:p.Val33Ala
XM_011529857.2:c.98T>C	XP_011528159.1:p.Val33Ala
XM_017028569.1:c.155T>C	XP_016884058.1:p.Val52Ala
XM_024452150.1:c.155T>C	XP_024307918.1:p.Val52Ala
XM_024452151.1:c.155T>C	XP_024307919.1:p.Val52Ala
XM_024452152.1:c.155T>C	XP_024307920.1:p.Val52Ala
XM_024452153.1:c.155T>C	XP_024307921.1:p.Val52Ala
XM_024452154.1:c.155T>C	XP_024307922.1:p.Val52Ala
XM_024452155.1:c.98T>C	XP_024307923.1:p.Val33Ala
NM_031910.4:c.155T>C MANE Select	NP_114116.3:p.Val52Ala
NM_182486.2:c.155T>C	NP_872292.1:p.Val52Ala