Canonical Allele Identifier: CA514767834

Gene: C1QTNF6

Linked Data

• MyVariant Identifiers: chr22:g.37581421A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37185381A>G , CM000684.2:g.37185381A>G	GRCh38
NC_000022.10:g.37581421A>G , CM000684.1:g.37581421A>G	GRCh37
NC_000022.9:g.35911367A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337843.7:c.126T>C MANE Select	ENSP00000338812.2:p.Pro42=
ENST00000337843.6:c.126T>C	ENSP00000338812.2:p.Pro42=
ENST00000397110.6:c.126T>C	ENSP00000380299.2:p.Pro42=
ENST00000434784.1:c.126T>C	ENSP00000399243.1:p.Pro42=
ENST00000470655.5:n.3616T>C
ENST00000493023.1:n.568T>C
NM_031910.3:c.126T>C	NP_114116.3:p.Pro42=
NM_182486.1:c.126T>C	NP_872292.1:p.Pro42=
XM_006724125.2:c.69T>C	XP_006724188.1:p.Pro23=
XM_011529857.1:c.69T>C	XP_011528159.1:p.Pro23=
NM_001365878.1:c.69T>C	NP_001352807.1:p.Pro23=
XM_011529857.2:c.69T>C	XP_011528159.1:p.Pro23=
XM_017028569.1:c.126T>C	XP_016884058.1:p.Pro42=
XM_024452150.1:c.126T>C	XP_024307918.1:p.Pro42=
XM_024452151.1:c.126T>C	XP_024307919.1:p.Pro42=
XM_024452152.1:c.126T>C	XP_024307920.1:p.Pro42=
XM_024452153.1:c.126T>C	XP_024307921.1:p.Pro42=
XM_024452154.1:c.126T>C	XP_024307922.1:p.Pro42=
XM_024452155.1:c.69T>C	XP_024307923.1:p.Pro23=
NM_031910.4:c.126T>C MANE Select	NP_114116.3:p.Pro42=
NM_182486.2:c.126T>C	NP_872292.1:p.Pro42=