Canonical Allele Identifier: CA363616127

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132132T>C (hg19) ; chr6:g.33164355T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164355T>C , CM000668.2:g.33164355T>C	GRCh38
NC_000006.11:g.33132132T>C , CM000668.1:g.33132132T>C	GRCh37
NC_000006.10:g.33240110T>C	NCBI36
NG_011589.1:g.33114A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.788A>G
ENST00000341947.7:c.4982A>G MANE Select	ENSP00000339915.2:p.Asp1661Gly
ENST00000341947.6:c.4982A>G	ENSP00000339915.2:p.Asp1661Gly
ENST00000361917.5:c.4661A>G	ENSP00000355123.1:p.Asp1554Gly
ENST00000374708.8:c.4724A>G	ENSP00000363840.4:p.Asp1575Gly
ENST00000477772.1:n.772A>G
NM_080679.2:c.4661A>G	NP_542410.2:p.Asp1554Gly
NM_080680.2:c.4982A>G	NP_542411.2:p.Asp1661Gly
NM_080681.2:c.4724A>G	NP_542412.2:p.Asp1575Gly
XM_011514298.1:c.4136A>G	XP_011512600.1:p.Asp1379Gly
XM_011514299.1:c.4268A>G	XP_011512601.1:p.Asp1423Gly
XM_011514300.1:c.4088A>G	XP_011512602.1:p.Asp1363Gly
XM_011514301.1:c.4025A>G	XP_011512603.1:p.Asp1342Gly
XM_011514302.1:c.3869A>G	XP_011512604.1:p.Asp1290Gly
XM_011514299.2:c.4268A>G	XP_011512601.1:p.Asp1423Gly
XM_011514300.2:c.4088A>G	XP_011512602.1:p.Asp1363Gly
XM_011514302.2:c.3869A>G	XP_011512604.1:p.Asp1290Gly
XM_017010250.1:c.4982A>G	XP_016865739.1:p.Asp1661Gly
XM_017010251.2:c.3800A>G	XP_016865740.1:p.Asp1267Gly
NM_080680.3:c.4982A>G MANE Select	NP_542411.2:p.Asp1661Gly
NM_080681.3:c.4724A>G	NP_542412.2:p.Asp1575Gly
NM_080679.3:c.4661A>G	NP_542410.2:p.Asp1554Gly