Canonical Allele Identifier: CA363616216

Gene: COL11A2

Linked Data

• ClinVar Variation Id: 2115442
• ClinVar RCV Id: RCV003032663
• MyVariant Identifiers: chr6:g.33132151A>C (hg19) ; chr6:g.33164374A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164374A>C , CM000668.2:g.33164374A>C	GRCh38
NC_000006.11:g.33132151A>C , CM000668.1:g.33132151A>C	GRCh37
NC_000006.10:g.33240129A>C	NCBI36
NG_011589.1:g.33095T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.769T>G
ENST00000341947.7:c.4963T>G MANE Select	ENSP00000339915.2:p.Cys1655Gly
ENST00000341947.6:c.4963T>G	ENSP00000339915.2:p.Cys1655Gly
ENST00000361917.5:c.4642T>G	ENSP00000355123.1:p.Cys1548Gly
ENST00000374708.8:c.4705T>G	ENSP00000363840.4:p.Cys1569Gly
ENST00000477772.1:n.753T>G
NM_080679.2:c.4642T>G	NP_542410.2:p.Cys1548Gly
NM_080680.2:c.4963T>G	NP_542411.2:p.Cys1655Gly
NM_080681.2:c.4705T>G	NP_542412.2:p.Cys1569Gly
XM_011514298.1:c.4117T>G	XP_011512600.1:p.Cys1373Gly
XM_011514299.1:c.4249T>G	XP_011512601.1:p.Cys1417Gly
XM_011514300.1:c.4069T>G	XP_011512602.1:p.Cys1357Gly
XM_011514301.1:c.4006T>G	XP_011512603.1:p.Cys1336Gly
XM_011514302.1:c.3850T>G	XP_011512604.1:p.Cys1284Gly
XM_011514299.2:c.4249T>G	XP_011512601.1:p.Cys1417Gly
XM_011514300.2:c.4069T>G	XP_011512602.1:p.Cys1357Gly
XM_011514302.2:c.3850T>G	XP_011512604.1:p.Cys1284Gly
XM_017010250.1:c.4963T>G	XP_016865739.1:p.Cys1655Gly
XM_017010251.2:c.3781T>G	XP_016865740.1:p.Cys1261Gly
NM_080680.3:c.4963T>G MANE Select	NP_542411.2:p.Cys1655Gly
NM_080681.3:c.4705T>G	NP_542412.2:p.Cys1569Gly
NM_080679.3:c.4642T>G	NP_542410.2:p.Cys1548Gly