Canonical Allele Identifier: CA2678226399
Gene: COL11A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33164506_33164507dup , CM000668.2:g.33164506_33164507dup GRCh38
NC_000006.11:g.33132283_33132284dup , CM000668.1:g.33132283_33132284dup GRCh37
NC_000006.10:g.33240261_33240262dup NCBI36
NG_011589.1:g.32965_32966dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000683572.1:n.670-31_670-30dup
ENST00000341947.7:c.4864-31_4864-30dup MANE Select ENSP00000339915.2:n.4864-31_4864-30dup
ENST00000341947.6:c.4864-31_4864-30dup ENSP00000339915.2:n.4864-31_4864-30dup
ENST00000361917.5:c.4543-31_4543-30dup ENSP00000355123.1:n.4543-31_4543-30dup
ENST00000374708.8:c.4606-31_4606-30dup ENSP00000363840.4:n.4606-31_4606-30dup
ENST00000477772.1:n.654-31_654-30dup
NM_080679.2:c.4543-31_4543-30dup NP_542410.2:n.4543-31_4543-30dup
NM_080680.2:c.4864-31_4864-30dup NP_542411.2:n.4864-31_4864-30dup
NM_080681.2:c.4606-31_4606-30dup NP_542412.2:n.4606-31_4606-30dup
XM_011514298.1:c.4018-31_4018-30dup XP_011512600.1:n.4018-31_4018-30dup
XM_011514299.1:c.4150-31_4150-30dup XP_011512601.1:n.4150-31_4150-30dup
XM_011514300.1:c.3970-31_3970-30dup XP_011512602.1:n.3970-31_3970-30dup
XM_011514301.1:c.3907-31_3907-30dup XP_011512603.1:n.3907-31_3907-30dup
XM_011514302.1:c.3751-31_3751-30dup XP_011512604.1:n.3751-31_3751-30dup
XM_011514299.2:c.4150-31_4150-30dup XP_011512601.1:n.4150-31_4150-30dup
XM_011514300.2:c.3970-31_3970-30dup XP_011512602.1:n.3970-31_3970-30dup
XM_011514302.2:c.3751-31_3751-30dup XP_011512604.1:n.3751-31_3751-30dup
XM_017010250.1:c.4864-31_4864-30dup XP_016865739.1:n.4864-31_4864-30dup
XM_017010251.2:c.3682-31_3682-30dup XP_016865740.1:n.3682-31_3682-30dup
NM_080680.3:c.4864-31_4864-30dup MANE Select NP_542411.2:n.4864-31_4864-30dup
NM_080681.3:c.4606-31_4606-30dup NP_542412.2:n.4606-31_4606-30dup
NM_080679.3:c.4543-31_4543-30dup NP_542410.2:n.4543-31_4543-30dup