Canonical Allele Identifier: CA2678226378
Gene: COL11A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33164503_33164504insTGGGAGAGAGAGGGCTGGCCTCAGAGGGGGAGAGAGAGGGCTGGCCTCAGAG , CM000668.2:g.33164503_33164504insTGGGAGAGAGAGGGCTGGCCTCAGAGGGGGAGAGAGAGGGCTGGCCTCAGAG GRCh38
NC_000006.11:g.33132280_33132281insTGGGAGAGAGAGGGCTGGCCTCAGAGGGGGAGAGAGAGGGCTGGCCTCAGAG , CM000668.1:g.33132280_33132281insTGGGAGAGAGAGGGCTGGCCTCAGAGGGGGAGAGAGAGGGCTGGCCTCAGAG GRCh37
NC_000006.10:g.33240258_33240259insTGGGAGAGAGAGGGCTGGCCTCAGAGGGGGAGAGAGAGGGCTGGCCTCAGAG NCBI36
NG_011589.1:g.32989_32990insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000683572.1:n.670-7_670-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC
ENST00000341947.7:c.4864-7_4864-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC MANE Select ENSP00000339915.2:n.4864-7_4864-6insCCCTCTGAGGCCAGCCCTCTCTCTC...
ENST00000341947.6:c.4864-7_4864-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC ENSP00000339915.2:n.4864-7_4864-6insCCCTCTGAGGCCAGCCCTCTCTCTC...
ENST00000361917.5:c.4543-7_4543-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC ENSP00000355123.1:n.4543-7_4543-6insCCCTCTGAGGCCAGCCCTCTCTCTC...
ENST00000374708.8:c.4606-7_4606-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC ENSP00000363840.4:n.4606-7_4606-6insCCCTCTGAGGCCAGCCCTCTCTCTC...
ENST00000477772.1:n.654-7_654-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC
NM_080679.2:c.4543-7_4543-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC NP_542410.2:n.4543-7_4543-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTC...
NM_080680.2:c.4864-7_4864-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC NP_542411.2:n.4864-7_4864-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTC...
NM_080681.2:c.4606-7_4606-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC NP_542412.2:n.4606-7_4606-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTC...
XM_011514298.1:c.4018-7_4018-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC XP_011512600.1:n.4018-7_4018-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCA...
XM_011514299.1:c.4150-7_4150-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC XP_011512601.1:n.4150-7_4150-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCA...
XM_011514300.1:c.3970-7_3970-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC XP_011512602.1:n.3970-7_3970-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCA...
XM_011514301.1:c.3907-7_3907-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC XP_011512603.1:n.3907-7_3907-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCA...
XM_011514302.1:c.3751-7_3751-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC XP_011512604.1:n.3751-7_3751-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCA...
XM_011514299.2:c.4150-7_4150-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC XP_011512601.1:n.4150-7_4150-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCA...
XM_011514300.2:c.3970-7_3970-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC XP_011512602.1:n.3970-7_3970-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCA...
XM_011514302.2:c.3751-7_3751-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC XP_011512604.1:n.3751-7_3751-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCA...
XM_017010250.1:c.4864-7_4864-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC XP_016865739.1:n.4864-7_4864-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCA...
XM_017010251.2:c.3682-7_3682-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC XP_016865740.1:n.3682-7_3682-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCA...
NM_080680.3:c.4864-7_4864-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC MANE Select NP_542411.2:n.4864-7_4864-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTC...
NM_080681.3:c.4606-7_4606-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC NP_542412.2:n.4606-7_4606-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTC...
NM_080679.3:c.4543-7_4543-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTCTGAGGCCAGCCCTCTCTCTCC NP_542410.2:n.4543-7_4543-6insCCCTCTGAGGCCAGCCCTCTCTCTCCCACTC...