Canonical Allele Identifier: CA3749967
Gene: COL11A2 HGNC NCBI

Linked Data

dbSNP Id: rs773243393

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33164486_33164489del , CM000668.2:g.33164486_33164489del GRCh38
NC_000006.11:g.33132263_33132266del , CM000668.1:g.33132263_33132266del GRCh37
NC_000006.10:g.33240241_33240244del NCBI36
NG_011589.1:g.32985_32988del

Transcript Alleles

HGVS Amino-acid Change
ENST00000683572.1:n.670-11_670-8del
ENST00000341947.7:c.4864-11_4864-8del MANE Select ENSP00000339915.2:n.4864-11_4864-8del
ENST00000341947.6:c.4864-11_4864-8del ENSP00000339915.2:n.4864-11_4864-8del
ENST00000361917.5:c.4543-11_4543-8del ENSP00000355123.1:n.4543-11_4543-8del
ENST00000374708.8:c.4606-11_4606-8del ENSP00000363840.4:n.4606-11_4606-8del
ENST00000477772.1:n.654-11_654-8del
NM_080679.2:c.4543-11_4543-8del NP_542410.2:n.4543-11_4543-8del
NM_080680.2:c.4864-11_4864-8del NP_542411.2:n.4864-11_4864-8del
NM_080681.2:c.4606-11_4606-8del NP_542412.2:n.4606-11_4606-8del
XM_011514298.1:c.4018-11_4018-8del XP_011512600.1:n.4018-11_4018-8del
XM_011514299.1:c.4150-11_4150-8del XP_011512601.1:n.4150-11_4150-8del
XM_011514300.1:c.3970-11_3970-8del XP_011512602.1:n.3970-11_3970-8del
XM_011514301.1:c.3907-11_3907-8del XP_011512603.1:n.3907-11_3907-8del
XM_011514302.1:c.3751-11_3751-8del XP_011512604.1:n.3751-11_3751-8del
XM_011514299.2:c.4150-11_4150-8del XP_011512601.1:n.4150-11_4150-8del
XM_011514300.2:c.3970-11_3970-8del XP_011512602.1:n.3970-11_3970-8del
XM_011514302.2:c.3751-11_3751-8del XP_011512604.1:n.3751-11_3751-8del
XM_017010250.1:c.4864-11_4864-8del XP_016865739.1:n.4864-11_4864-8del
XM_017010251.2:c.3682-11_3682-8del XP_016865740.1:n.3682-11_3682-8del
NM_080680.3:c.4864-11_4864-8del MANE Select NP_542411.2:n.4864-11_4864-8del
NM_080681.3:c.4606-11_4606-8del NP_542412.2:n.4606-11_4606-8del
NM_080679.3:c.4543-11_4543-8del NP_542410.2:n.4543-11_4543-8del