Canonical Allele Identifier: CA363617363

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132629C>G (hg19) ; chr6:g.33164852C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164852C>G , CM000668.2:g.33164852C>G	GRCh38
NC_000006.11:g.33132629C>G , CM000668.1:g.33132629C>G	GRCh37
NC_000006.10:g.33240607C>G	NCBI36
NG_011589.1:g.32617G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000683572.1:n.669G>C
ENST00000341947.7:c.4863G>C MANE Select	ENSP00000339915.2:p.Gln1621His
ENST00000341947.6:c.4863G>C	ENSP00000339915.2:p.Gln1621His
ENST00000361917.5:c.4542G>C	ENSP00000355123.1:p.Gln1514His
ENST00000374708.8:c.4605G>C	ENSP00000363840.4:p.Gln1535His
ENST00000477772.1:n.653G>C
NM_080679.2:c.4542G>C	NP_542410.2:p.Gln1514His
NM_080680.2:c.4863G>C	NP_542411.2:p.Gln1621His
NM_080681.2:c.4605G>C	NP_542412.2:p.Gln1535His
XM_011514298.1:c.4017G>C	XP_011512600.1:p.Gln1339His
XM_011514299.1:c.4149G>C	XP_011512601.1:p.Gln1383His
XM_011514300.1:c.3969G>C	XP_011512602.1:p.Gln1323His
XM_011514301.1:c.3906G>C	XP_011512603.1:p.Gln1302His
XM_011514302.1:c.3750G>C	XP_011512604.1:p.Gln1250His
XM_011514299.2:c.4149G>C	XP_011512601.1:p.Gln1383His
XM_011514300.2:c.3969G>C	XP_011512602.1:p.Gln1323His
XM_011514302.2:c.3750G>C	XP_011512604.1:p.Gln1250His
XM_017010250.1:c.4863G>C	XP_016865739.1:p.Gln1621His
XM_017010251.2:c.3681G>C	XP_016865740.1:p.Gln1227His
NM_080680.3:c.4863G>C MANE Select	NP_542411.2:p.Gln1621His
NM_080681.3:c.4605G>C	NP_542412.2:p.Gln1535His
NM_080679.3:c.4542G>C	NP_542410.2:p.Gln1514His