Canonical Allele Identifier: CA363617770

Gene: COL11A2

Linked Data

• dbSNP Id: rs1329672936
• gnomAD v2: 6-33132718-G-C
• gnomAD v4: 6-33164941-G-C
• MyVariant Identifiers: chr6:g.33132718G>C (hg19) ; chr6:g.33164941G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164941G>C , CM000668.2:g.33164941G>C	GRCh38
NC_000006.11:g.33132718G>C , CM000668.1:g.33132718G>C	GRCh37
NC_000006.10:g.33240696G>C	NCBI36
NG_011589.1:g.32528C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.580C>G
ENST00000341947.7:c.4774C>G MANE Select	ENSP00000339915.2:p.Gln1592Glu
ENST00000341947.6:c.4774C>G	ENSP00000339915.2:p.Gln1592Glu
ENST00000361917.5:c.4453C>G	ENSP00000355123.1:p.Gln1485Glu
ENST00000374708.8:c.4516C>G	ENSP00000363840.4:p.Gln1506Glu
ENST00000477772.1:n.564C>G
NM_080679.2:c.4453C>G	NP_542410.2:p.Gln1485Glu
NM_080680.2:c.4774C>G	NP_542411.2:p.Gln1592Glu
NM_080681.2:c.4516C>G	NP_542412.2:p.Gln1506Glu
XM_011514298.1:c.3928C>G	XP_011512600.1:p.Gln1310Glu
XM_011514299.1:c.4060C>G	XP_011512601.1:p.Gln1354Glu
XM_011514300.1:c.3880C>G	XP_011512602.1:p.Gln1294Glu
XM_011514301.1:c.3817C>G	XP_011512603.1:p.Gln1273Glu
XM_011514302.1:c.3661C>G	XP_011512604.1:p.Gln1221Glu
XM_011514299.2:c.4060C>G	XP_011512601.1:p.Gln1354Glu
XM_011514300.2:c.3880C>G	XP_011512602.1:p.Gln1294Glu
XM_011514302.2:c.3661C>G	XP_011512604.1:p.Gln1221Glu
XM_017010250.1:c.4774C>G	XP_016865739.1:p.Gln1592Glu
XM_017010251.2:c.3592C>G	XP_016865740.1:p.Gln1198Glu
NM_080680.3:c.4774C>G MANE Select	NP_542411.2:p.Gln1592Glu
NM_080681.3:c.4516C>G	NP_542412.2:p.Gln1506Glu
NM_080679.3:c.4453C>G	NP_542410.2:p.Gln1485Glu