Canonical Allele Identifier: CA1619890441
Gene: COL11A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33164868C= , CM000668.2:g.33164868C= GRCh38
NC_000006.11:g.33132645C= , CM000668.1:g.33132645C= GRCh37
NC_000006.10:g.33240623C= NCBI36
NG_011589.1:g.32601G=

Transcript Alleles

HGVS Amino-acid change
ENST00000683572.1:n.653G=
ENST00000341947.7:c.4847G= MANE Select ENSP00000339915.2:p.Arg1616=
ENST00000341947.6:c.4847G= ENSP00000339915.2:p.Arg1616=
ENST00000361917.5:c.4526G= ENSP00000355123.1:p.Arg1509=
ENST00000374708.8:c.4589G= ENSP00000363840.4:p.Arg1530=
ENST00000477772.1:n.637G=
NM_080679.2:c.4526G= NP_542410.2:p.Arg1509=
NM_080680.2:c.4847G= NP_542411.2:p.Arg1616=
NM_080681.2:c.4589G= NP_542412.2:p.Arg1530=
XM_011514298.1:c.4001G= XP_011512600.1:p.Arg1334=
XM_011514299.1:c.4133G= XP_011512601.1:p.Arg1378=
XM_011514300.1:c.3953G= XP_011512602.1:p.Arg1318=
XM_011514301.1:c.3890G= XP_011512603.1:p.Arg1297=
XM_011514302.1:c.3734G= XP_011512604.1:p.Arg1245=
XM_011514299.2:c.4133G= XP_011512601.1:p.Arg1378=
XM_011514300.2:c.3953G= XP_011512602.1:p.Arg1318=
XM_011514302.2:c.3734G= XP_011512604.1:p.Arg1245=
XM_017010250.1:c.4847G= XP_016865739.1:p.Arg1616=
XM_017010251.2:c.3665G= XP_016865740.1:p.Arg1222=
NM_080680.3:c.4847G= MANE Select NP_542411.2:p.Arg1616=
NM_080681.3:c.4589G= NP_542412.2:p.Arg1530=
NM_080679.3:c.4526G= NP_542410.2:p.Arg1509=