Canonical Allele Identifier: CA1815060133

Gene: COL14A1

Linked Data

• dbSNP Id: rs10955961

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.120206362T>A , CM000670.2:g.120206362T>A	GRCh38
NC_000008.10:g.121218601T>A , CM000670.1:g.121218601T>A	GRCh37
NC_000008.9:g.121287782T>A	NCBI36
NG_033107.1:g.86255T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000297848.8:c.1040-581T>A MANE Select	ENSP00000297848.3:n.1040-581T>A
ENST00000297848.7:c.1040-581T>A	ENSP00000297848.3:n.1040-581T>A
ENST00000309791.8:c.1040-581T>A	ENSP00000311809.4:n.1040-581T>A
ENST00000432943.6:n.1274-581T>A
ENST00000434620.5:c.479-581T>A	ENSP00000409461.1:n.479-581T>A
ENST00000498051.6:c.1040-581T>A	ENSP00000428851.1:n.1040-581T>A
ENST00000523142.5:c.309-581T>A
ENST00000537875.2:c.1040-581T>A	ENSP00000443974.1:n.1040-581T>A
NM_021110.2:c.1040-581T>A	NP_066933.1:n.1040-581T>A
XM_005251059.2:c.1040-581T>A	XP_005251116.1:n.1040-581T>A
XM_006716651.2:c.1040-581T>A	XP_006716714.1:n.1040-581T>A
NM_021110.3:c.1040-581T>A	NP_066933.1:n.1040-581T>A
XM_005251059.4:c.1040-581T>A	XP_005251116.1:n.1040-581T>A
XM_006716651.3:c.1040-581T>A	XP_006716714.1:n.1040-581T>A
XM_017013809.2:c.1040-581T>A	XP_016869298.1:n.1040-581T>A
NM_021110.4:c.1040-581T>A MANE Select	NP_066933.1:n.1040-581T>A
NM_001384947.1:c.1040-581T>A	NP_001371876.1:n.1040-581T>A