Canonical Allele Identifier: CA1619898443
Gene: COL11A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33174554A= , CM000668.2:g.33174554A= GRCh38
NC_000006.11:g.33142331A= , CM000668.1:g.33142331A= GRCh37
NC_000006.10:g.33250309A= NCBI36
NG_011589.1:g.22915T=

Transcript Alleles

HGVS Amino-acid change
ENST00000361917.6:c.976T=
ENST00000341947.7:c.2403T= MANE Select ENSP00000339915.2:p.Pro801=
ENST00000341947.6:c.2403T= ENSP00000339915.2:p.Pro801=
ENST00000361917.5:c.2082T= ENSP00000355123.1:p.Pro694=
ENST00000374708.8:c.2145T= ENSP00000363840.4:p.Pro715=
ENST00000477772.1:n.272+2455T=
NM_080679.2:c.2082T= NP_542410.2:p.Pro694=
NM_080680.2:c.2403T= NP_542411.2:p.Pro801=
NM_080681.2:c.2145T= NP_542412.2:p.Pro715=
XM_011514298.1:c.1557T= XP_011512600.1:p.Pro519=
XM_011514299.1:c.1689T= XP_011512601.1:p.Pro563=
XM_011514300.1:c.1509T= XP_011512602.1:p.Pro503=
XM_011514301.1:c.1446T= XP_011512603.1:p.Pro482=
XM_011514302.1:c.1290T= XP_011512604.1:p.Pro430=
XM_011514299.2:c.1689T= XP_011512601.1:p.Pro563=
XM_011514300.2:c.1509T= XP_011512602.1:p.Pro503=
XM_011514302.2:c.1290T= XP_011512604.1:p.Pro430=
XM_017010250.1:c.2403T= XP_016865739.1:p.Pro801=
XM_017010251.2:c.1221T= XP_016865740.1:p.Pro407=
NM_080680.3:c.2403T= MANE Select NP_542411.2:p.Pro801=
NM_080681.3:c.2145T= NP_542412.2:p.Pro715=
NM_080679.3:c.2082T= NP_542410.2:p.Pro694=