Canonical Allele Identifier: CA1619898440
Gene: COL11A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33174545A= , CM000668.2:g.33174545A= GRCh38
NC_000006.11:g.33142322A= , CM000668.1:g.33142322A= GRCh37
NC_000006.10:g.33250300A= NCBI36
NG_011589.1:g.22924T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361917.6:c.985T=
ENST00000341947.7:c.2412T= MANE Select ENSP00000339915.2:p.Pro804=
ENST00000341947.6:c.2412T= ENSP00000339915.2:p.Pro804=
ENST00000361917.5:c.2091T= ENSP00000355123.1:p.Pro697=
ENST00000374708.8:c.2154T= ENSP00000363840.4:p.Pro718=
ENST00000477772.1:n.272+2464T=
NM_080679.2:c.2091T= NP_542410.2:p.Pro697=
NM_080680.2:c.2412T= NP_542411.2:p.Pro804=
NM_080681.2:c.2154T= NP_542412.2:p.Pro718=
XM_011514298.1:c.1566T= XP_011512600.1:p.Pro522=
XM_011514299.1:c.1698T= XP_011512601.1:p.Pro566=
XM_011514300.1:c.1518T= XP_011512602.1:p.Pro506=
XM_011514301.1:c.1455T= XP_011512603.1:p.Pro485=
XM_011514302.1:c.1299T= XP_011512604.1:p.Pro433=
XM_011514299.2:c.1698T= XP_011512601.1:p.Pro566=
XM_011514300.2:c.1518T= XP_011512602.1:p.Pro506=
XM_011514302.2:c.1299T= XP_011512604.1:p.Pro433=
XM_017010250.1:c.2412T= XP_016865739.1:p.Pro804=
XM_017010251.2:c.1230T= XP_016865740.1:p.Pro410=
NM_080680.3:c.2412T= MANE Select NP_542411.2:p.Pro804=
NM_080681.3:c.2154T= NP_542412.2:p.Pro718=
NM_080679.3:c.2091T= NP_542410.2:p.Pro697=