Canonical Allele Identifier: CA1619890436
Gene: COL11A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33164866C= , CM000668.2:g.33164866C= GRCh38
NC_000006.11:g.33132643C= , CM000668.1:g.33132643C= GRCh37
NC_000006.10:g.33240621C= NCBI36
NG_011589.1:g.32603G=

Transcript Alleles

HGVS Amino-acid change
ENST00000683572.1:n.655G=
ENST00000341947.7:c.4849G= MANE Select ENSP00000339915.2:p.Asp1617=
ENST00000341947.6:c.4849G= ENSP00000339915.2:p.Asp1617=
ENST00000361917.5:c.4528G= ENSP00000355123.1:p.Asp1510=
ENST00000374708.8:c.4591G= ENSP00000363840.4:p.Asp1531=
ENST00000477772.1:n.639G=
NM_080679.2:c.4528G= NP_542410.2:p.Asp1510=
NM_080680.2:c.4849G= NP_542411.2:p.Asp1617=
NM_080681.2:c.4591G= NP_542412.2:p.Asp1531=
XM_011514298.1:c.4003G= XP_011512600.1:p.Asp1335=
XM_011514299.1:c.4135G= XP_011512601.1:p.Asp1379=
XM_011514300.1:c.3955G= XP_011512602.1:p.Asp1319=
XM_011514301.1:c.3892G= XP_011512603.1:p.Asp1298=
XM_011514302.1:c.3736G= XP_011512604.1:p.Asp1246=
XM_011514299.2:c.4135G= XP_011512601.1:p.Asp1379=
XM_011514300.2:c.3955G= XP_011512602.1:p.Asp1319=
XM_011514302.2:c.3736G= XP_011512604.1:p.Asp1246=
XM_017010250.1:c.4849G= XP_016865739.1:p.Asp1617=
XM_017010251.2:c.3667G= XP_016865740.1:p.Asp1223=
NM_080680.3:c.4849G= MANE Select NP_542411.2:p.Asp1617=
NM_080681.3:c.4591G= NP_542412.2:p.Asp1531=
NM_080679.3:c.4528G= NP_542410.2:p.Asp1510=