Canonical Allele Identifier: CA466775018

Gene: COL27A1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114162751C>T , CM000671.2:g.114162751C>T	GRCh38
NC_000009.11:g.116925031C>T , CM000671.1:g.116925031C>T	GRCh37
NC_000009.10:g.115964852C>T	NCBI36
NG_034260.1:g.12207C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356083.8:c.99C>T MANE Select	ENSP00000348385.3:p.Ala33=
ENST00000356083.7:c.99C>T	ENSP00000348385.3:p.Ala33=
NM_032888.3:c.99C>T	NP_116277.2:p.Ala33=
XM_006717308.2:c.99C>T	XP_006717371.1:p.Ala33=
XM_011519138.1:c.93C>T	XP_011517440.1:p.Ala31=
XM_011519139.1:c.75C>T	XP_011517441.1:p.Ala25=
XM_011519140.1:c.99C>T	XP_011517442.1:p.Ala33=
XM_011519141.1:c.99C>T	XP_011517443.1:p.Ala33=
XM_011519142.1:c.99C>T	XP_011517444.1:p.Ala33=
XM_011519143.1:c.99C>T	XP_011517445.1:p.Ala33=
XM_011519144.1:c.99C>T	XP_011517446.1:p.Ala33=
XR_929860.1:n.575C>T
XR_929861.1:n.576C>T
XR_929862.1:n.577C>T
XR_929863.1:n.577C>T
XM_011519138.2:c.93C>T	XP_011517440.1:p.Ala31=
XM_011519142.3:c.99C>T	XP_011517444.1:p.Ala33=
XM_011519143.2:c.99C>T	XP_011517445.1:p.Ala33=
XM_011519144.2:c.99C>T	XP_011517446.1:p.Ala33=
XM_017015239.1:c.99C>T	XP_016870728.1:p.Ala33=
XR_001746405.1:n.577C>T
XR_929860.3:n.576C>T
XR_929861.2:n.577C>T
NM_032888.4:c.99C>T MANE Select	NP_116277.2:p.Ala33=