Canonical Allele Identifier: CA137054944

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33192322G>C , CM000668.2:g.33192322G>C	GRCh38
NC_000006.11:g.33160099G>C , CM000668.1:g.33160099G>C	GRCh37
NC_000006.10:g.33268077G>C	NCBI36
NG_011589.1:g.5147C>G
NG_023374.1:g.13334C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_080680.3:c.-82C>G MANE Select	NP_542411.2:n.-82C>G
ENST00000341947.7:c.-82C>G MANE Select	ENSP00000339915.2:n.-82C>G
NM_001163771.1:c.-82C>G	NP_001157243.1:n.-82C>G
NM_001163771.2:c.-82C>G	NP_001157243.1:n.-82C>G
NM_080679.2:c.-82C>G	NP_542410.2:n.-82C>G
NM_080679.3:c.-82C>G	NP_542410.2:n.-82C>G
NM_080680.2:c.-82C>G	NP_542411.2:n.-82C>G
NM_080681.2:c.-82C>G	NP_542412.2:n.-82C>G
NM_080681.3:c.-82C>G	NP_542412.2:n.-82C>G
ENST00000341947.6:c.-82C>G	ENSP00000339915.2:n.-82C>G
ENST00000361917.5:c.-82C>G	ENSP00000355123.1:n.-82C>G
ENST00000374708.8:c.-82C>G	ENSP00000363840.4:n.-82C>G
ENST00000395194.1:c.-82C>G	ENSP00000378620.1:n.-82C>G
ENST00000457788.5:c.-82C>G	ENSP00000405520.1:n.-82C>G
XM_011514298.1:c.-765+703C>G	XP_011512600.1:n.-765+703C>G
XM_017010250.1:c.-66-16C>G	XP_016865739.1:n.-66-16C>G