Canonical Allele Identifier: CA1619898441
Gene: COL11A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33174549T= , CM000668.2:g.33174549T= GRCh38
NC_000006.11:g.33142326T= , CM000668.1:g.33142326T= GRCh37
NC_000006.10:g.33250304T= NCBI36
NG_011589.1:g.22920A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361917.6:c.981A=
ENST00000341947.7:c.2408A= MANE Select ENSP00000339915.2:p.Tyr803=
ENST00000341947.6:c.2408A= ENSP00000339915.2:p.Tyr803=
ENST00000361917.5:c.2087A= ENSP00000355123.1:p.Tyr696=
ENST00000374708.8:c.2150A= ENSP00000363840.4:p.Tyr717=
ENST00000477772.1:n.272+2460A=
NM_080679.2:c.2087A= NP_542410.2:p.Tyr696=
NM_080680.2:c.2408A= NP_542411.2:p.Tyr803=
NM_080681.2:c.2150A= NP_542412.2:p.Tyr717=
XM_011514298.1:c.1562A= XP_011512600.1:p.Tyr521=
XM_011514299.1:c.1694A= XP_011512601.1:p.Tyr565=
XM_011514300.1:c.1514A= XP_011512602.1:p.Tyr505=
XM_011514301.1:c.1451A= XP_011512603.1:p.Tyr484=
XM_011514302.1:c.1295A= XP_011512604.1:p.Tyr432=
XM_011514299.2:c.1694A= XP_011512601.1:p.Tyr565=
XM_011514300.2:c.1514A= XP_011512602.1:p.Tyr505=
XM_011514302.2:c.1295A= XP_011512604.1:p.Tyr432=
XM_017010250.1:c.2408A= XP_016865739.1:p.Tyr803=
XM_017010251.2:c.1226A= XP_016865740.1:p.Tyr409=
NM_080680.3:c.2408A= MANE Select NP_542411.2:p.Tyr803=
NM_080681.3:c.2150A= NP_542412.2:p.Tyr717=
NM_080679.3:c.2087A= NP_542410.2:p.Tyr696=