Canonical Allele Identifier: CA4858626

Gene: COL14A1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.120197830T>C , CM000670.2:g.120197830T>C	GRCh38
NC_000008.10:g.121210069T>C , CM000670.1:g.121210069T>C	GRCh37
NC_000008.9:g.121279250T>C	NCBI36
NG_033107.1:g.77723T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297848.8:c.612T>C MANE Select	ENSP00000297848.3:p.Gly204=
ENST00000297848.7:c.612T>C	ENSP00000297848.3:p.Gly204=
ENST00000309791.8:c.612T>C	ENSP00000311809.4:p.Gly204=
ENST00000432943.6:n.846T>C
ENST00000434620.5:c.51T>C	ENSP00000409461.1:p.Gly17=
ENST00000498051.6:c.612T>C	ENSP00000428851.1:p.Gly204=
ENST00000523142.5:c.146+884T>C
ENST00000537875.2:c.612T>C	ENSP00000443974.1:p.Gly204=
NM_021110.2:c.612T>C	NP_066933.1:p.Gly204=
XM_005251059.2:c.612T>C	XP_005251116.1:p.Gly204=
XM_006716651.2:c.612T>C	XP_006716714.1:p.Gly204=
NM_021110.3:c.612T>C	NP_066933.1:p.Gly204=
XM_005251059.4:c.612T>C	XP_005251116.1:p.Gly204=
XM_006716651.3:c.612T>C	XP_006716714.1:p.Gly204=
XM_017013809.2:c.612T>C	XP_016869298.1:p.Gly204=
NM_021110.4:c.612T>C MANE Select	NP_066933.1:p.Gly204=
NM_001384947.1:c.612T>C	NP_001371876.1:p.Gly204=