Canonical Allele Identifier: CA1619899082
Gene: COL11A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33176171C= , CM000668.2:g.33176171C= GRCh38
NC_000006.11:g.33143948C= , CM000668.1:g.33143948C= GRCh37
NC_000006.10:g.33251926C= NCBI36
NG_011589.1:g.21298G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361917.6:c.787+88G=
ENST00000341947.7:c.2214+88G= MANE Select ENSP00000339915.2:n.2214+88G=
ENST00000341947.6:c.2214+88G= ENSP00000339915.2:n.2214+88G=
ENST00000361917.5:c.1893+88G= ENSP00000355123.1:n.1893+88G=
ENST00000374708.8:c.1956+88G= ENSP00000363840.4:n.1956+88G=
ENST00000477772.1:n.272+838G=
NM_080679.2:c.1893+88G= NP_542410.2:n.1893+88G=
NM_080680.2:c.2214+88G= NP_542411.2:n.2214+88G=
NM_080681.2:c.1956+88G= NP_542412.2:n.1956+88G=
XM_011514298.1:c.1368+88G= XP_011512600.1:n.1368+88G=
XM_011514299.1:c.1500+88G= XP_011512601.1:n.1500+88G=
XM_011514300.1:c.1320+88G= XP_011512602.1:n.1320+88G=
XM_011514301.1:c.1257+88G= XP_011512603.1:n.1257+88G=
XM_011514302.1:c.1101+88G= XP_011512604.1:n.1101+88G=
XM_011514299.2:c.1500+88G= XP_011512601.1:n.1500+88G=
XM_011514300.2:c.1320+88G= XP_011512602.1:n.1320+88G=
XM_011514302.2:c.1101+88G= XP_011512604.1:n.1101+88G=
XM_017010250.1:c.2214+88G= XP_016865739.1:n.2214+88G=
XM_017010251.2:c.1032+88G= XP_016865740.1:n.1032+88G=
NM_080680.3:c.2214+88G= MANE Select NP_542411.2:n.2214+88G=
NM_080681.3:c.1956+88G= NP_542412.2:n.1956+88G=
NM_080679.3:c.1893+88G= NP_542410.2:n.1893+88G=