Canonical Allele Identifier: CA363609657

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33153532G>C (hg19) ; chr6:g.33185755G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33185755G>C , CM000668.2:g.33185755G>C	GRCh38
NC_000006.11:g.33153532G>C , CM000668.1:g.33153532G>C	GRCh37
NC_000006.10:g.33261510G>C	NCBI36
NG_011589.1:g.11714C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682718.1:n.639C>G
ENST00000341947.7:c.822C>G MANE Select	ENSP00000339915.2:p.Asp274Glu
ENST00000341947.6:c.822C>G	ENSP00000339915.2:p.Asp274Glu
ENST00000361917.5:c.798+872C>G	ENSP00000355123.1:n.798+872C>G
ENST00000374708.8:c.799-701C>G	ENSP00000363840.4:n.799-701C>G
ENST00000457788.5:c.822C>G	ENSP00000405520.1:p.Asp274Glu
NM_080679.2:c.798+872C>G	NP_542410.2:n.798+872C>G
NM_080680.2:c.822C>G	NP_542411.2:p.Asp274Glu
NM_080681.2:c.799-701C>G	NP_542412.2:n.799-701C>G
XM_011514298.1:c.-25C>G	XP_011512600.1:n.-25C>G
XM_017010250.1:c.822C>G	XP_016865739.1:p.Asp274Glu
NM_080680.3:c.822C>G MANE Select	NP_542411.2:p.Asp274Glu
NM_080681.3:c.799-701C>G	NP_542412.2:n.799-701C>G
NM_080679.3:c.798+872C>G	NP_542410.2:n.798+872C>G