Canonical Allele Identifier: CA466776230

Gene: COL27A1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114155971G>C , CM000671.2:g.114155971G>C	GRCh38
NC_000009.11:g.116918251G>C , CM000671.1:g.116918251G>C	GRCh37
NC_000009.10:g.115958072G>C	NCBI36
NG_034260.1:g.5427G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356083.8:c.21G>C MANE Select	ENSP00000348385.3:p.Arg7=
ENST00000356083.7:c.21G>C	ENSP00000348385.3:p.Arg7=
NM_032888.3:c.21G>C	NP_116277.2:p.Arg7=
XM_006717308.2:c.21G>C	XP_006717371.1:p.Arg7=
XM_011519138.1:c.56+1601G>C	XP_011517440.1:n.56+1601G>C
XM_011519139.1:c.39-6744G>C	XP_011517441.1:n.39-6744G>C
XM_011519140.1:c.21G>C	XP_011517442.1:p.Arg7=
XM_011519141.1:c.21G>C	XP_011517443.1:p.Arg7=
XM_011519142.1:c.21G>C	XP_011517444.1:p.Arg7=
XM_011519143.1:c.21G>C	XP_011517445.1:p.Arg7=
XM_011519144.1:c.21G>C	XP_011517446.1:p.Arg7=
XR_929860.1:n.497G>C
XR_929861.1:n.498G>C
XR_929862.1:n.499G>C
XR_929863.1:n.499G>C
XM_011519138.2:c.56+1601G>C	XP_011517440.1:n.56+1601G>C
XM_011519142.3:c.21G>C	XP_011517444.1:p.Arg7=
XM_011519143.2:c.21G>C	XP_011517445.1:p.Arg7=
XM_011519144.2:c.21G>C	XP_011517446.1:p.Arg7=
XM_017015239.1:c.21G>C	XP_016870728.1:p.Arg7=
XR_001746405.1:n.499G>C
XR_929860.3:n.498G>C
XR_929861.2:n.499G>C
NM_032888.4:c.21G>C MANE Select	NP_116277.2:p.Arg7=