Canonical Allele Identifier: CA1619897107
Gene: COL11A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33171558A= , CM000668.2:g.33171558A= GRCh38
NC_000006.11:g.33139335A= , CM000668.1:g.33139335A= GRCh37
NC_000006.10:g.33247313A= NCBI36
NG_011589.1:g.25911T=

Transcript Alleles

HGVS Amino-acid change
ENST00000341947.7:c.3167T= MANE Select ENSP00000339915.2:p.Ile1056=
ENST00000341947.6:c.3167T= ENSP00000339915.2:p.Ile1056=
ENST00000361917.5:c.2846T= ENSP00000355123.1:p.Ile949=
ENST00000374708.8:c.2909T= ENSP00000363840.4:p.Ile970=
ENST00000477772.1:n.272+5451T=
NM_080679.2:c.2846T= NP_542410.2:p.Ile949=
NM_080680.2:c.3167T= NP_542411.2:p.Ile1056=
NM_080681.2:c.2909T= NP_542412.2:p.Ile970=
XM_011514298.1:c.2321T= XP_011512600.1:p.Ile774=
XM_011514299.1:c.2453T= XP_011512601.1:p.Ile818=
XM_011514300.1:c.2273T= XP_011512602.1:p.Ile758=
XM_011514301.1:c.2210T= XP_011512603.1:p.Ile737=
XM_011514302.1:c.2054T= XP_011512604.1:p.Ile685=
XM_011514299.2:c.2453T= XP_011512601.1:p.Ile818=
XM_011514300.2:c.2273T= XP_011512602.1:p.Ile758=
XM_011514302.2:c.2054T= XP_011512604.1:p.Ile685=
XM_017010250.1:c.3167T= XP_016865739.1:p.Ile1056=
XM_017010251.2:c.1985T= XP_016865740.1:p.Ile662=
NM_080680.3:c.3167T= MANE Select NP_542411.2:p.Ile1056=
NM_080681.3:c.2909T= NP_542412.2:p.Ile970=
NM_080679.3:c.2846T= NP_542410.2:p.Ile949=