Canonical Allele Identifier: CA1484355230

Gene: COL25A1

Linked Data

• dbSNP Id: rs13134663

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108919403A>C , CM000666.2:g.108919403A>C	GRCh38
NC_000004.11:g.109840559A>C , CM000666.1:g.109840559A>C	GRCh37
NC_000004.10:g.110060008A>C	NCBI36
NG_047204.1:g.388350T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399132.6:c.735+1175T>G MANE Select	ENSP00000382083.1:n.735+1175T>G
ENST00000642955.1:c.735+1175T>G	ENSP00000495847.1:n.735+1175T>G
ENST00000399126.1:c.735+1175T>G	ENSP00000382077.1:n.735+1175T>G
ENST00000399127.5:c.723+1175T>G	ENSP00000382078.1:n.723+1175T>G
ENST00000399132.5:c.735+1175T>G	ENSP00000382083.1:n.735+1175T>G
ENST00000494183.5:c.519+1175T>G	ENSP00000437131.1:n.519+1175T>G
ENST00000610288.4:c.30+1175T>G	ENSP00000482699.1:n.30+1175T>G
ENST00000622134.4:c.249+1175T>G	ENSP00000484110.1:n.249+1175T>G
NM_001256074.1:c.723+1175T>G	NP_001243003.1:n.723+1175T>G
NM_032518.2:c.735+1175T>G	NP_115907.2:n.735+1175T>G
NM_198721.3:c.735+1175T>G	NP_942014.1:n.735+1175T>G
NR_045756.2:n.640+1175T>G
XM_011532332.1:c.735+1175T>G	XP_011530634.1:n.735+1175T>G
XM_011532333.1:c.735+1175T>G	XP_011530635.1:n.735+1175T>G
XM_011532334.1:c.735+1175T>G	XP_011530636.1:n.735+1175T>G
XM_011532335.1:c.735+1175T>G	XP_011530637.1:n.735+1175T>G
XM_011532336.1:c.735+1175T>G	XP_011530638.1:n.735+1175T>G
XM_011532337.1:c.723+1175T>G	XP_011530639.1:n.723+1175T>G
XM_011532338.1:c.717+1175T>G	XP_011530640.1:n.717+1175T>G
XM_011532339.1:c.735+1175T>G	XP_011530641.1:n.735+1175T>G
XM_011532340.1:c.735+1175T>G	XP_011530642.1:n.735+1175T>G
XM_011532341.1:c.705+1175T>G	XP_011530643.1:n.705+1175T>G
XM_011532342.1:c.735+1175T>G	XP_011530644.1:n.735+1175T>G
XM_011532343.1:c.735+1175T>G	XP_011530645.1:n.735+1175T>G
XM_011532344.1:c.663+1175T>G	XP_011530646.1:n.663+1175T>G
XM_011532345.1:c.735+1175T>G	XP_011530647.1:n.735+1175T>G
XM_011532346.1:c.735+1175T>G	XP_011530648.1:n.735+1175T>G
XM_011532347.1:c.735+1175T>G	XP_011530649.1:n.735+1175T>G
XM_011532348.1:c.735+1175T>G	XP_011530650.1:n.735+1175T>G
XM_011532349.1:c.735+1175T>G	XP_011530651.1:n.735+1175T>G
XM_011532350.1:c.735+1175T>G	XP_011530652.1:n.735+1175T>G
XM_011532351.1:c.735+1175T>G	XP_011530653.1:n.735+1175T>G
XM_011532352.1:c.735+1175T>G	XP_011530654.1:n.735+1175T>G
XM_011532353.1:c.735+1175T>G	XP_011530655.1:n.735+1175T>G
XM_011532354.1:c.435+1175T>G	XP_011530656.1:n.435+1175T>G
XM_011532355.1:c.396+1175T>G	XP_011530657.1:n.396+1175T>G
XM_011532356.1:c.378+1175T>G	XP_011530658.1:n.378+1175T>G
XM_011532357.1:c.735+1175T>G	XP_011530659.1:n.735+1175T>G
XM_011532358.1:c.252+1175T>G	XP_011530660.1:n.252+1175T>G
XM_011532359.1:c.735+1175T>G	XP_011530661.1:n.735+1175T>G
XR_938784.1:n.1468+1175T>G
XR_938785.1:n.1468+1175T>G
XR_938786.1:n.1468+1175T>G
XR_938787.1:n.1468+1175T>G
XR_938788.1:n.1468+1175T>G
XM_011532333.2:c.735+1175T>G	XP_011530635.1:n.735+1175T>G
XM_011532334.2:c.735+1175T>G	XP_011530636.1:n.735+1175T>G
XM_011532335.2:c.735+1175T>G	XP_011530637.1:n.735+1175T>G
XM_011532338.2:c.717+1175T>G	XP_011530640.1:n.717+1175T>G
XM_011532355.2:c.396+1175T>G	XP_011530657.1:n.396+1175T>G
XM_011532356.2:c.378+1175T>G	XP_011530658.1:n.378+1175T>G
XM_011532358.2:c.252+1175T>G	XP_011530660.1:n.252+1175T>G
XM_017008735.1:c.717+1175T>G	XP_016864224.1:n.717+1175T>G
XM_017008736.1:c.735+1175T>G	XP_016864225.1:n.735+1175T>G
XM_017008737.1:c.396+1175T>G	XP_016864226.1:n.396+1175T>G
NM_198721.4:c.735+1175T>G MANE Select	NP_942014.1:n.735+1175T>G
NM_001256074.2:c.723+1175T>G	NP_001243003.1:n.723+1175T>G
NM_032518.3:c.735+1175T>G	NP_115907.2:n.735+1175T>G
NR_045756.3:n.931+1175T>G
NM_001256074.3:c.723+1175T>G	NP_001243003.1:n.723+1175T>G
NM_032518.4:c.735+1175T>G	NP_115907.2:n.735+1175T>G