Canonical Allele Identifier: CA363634671
Gene: COL11A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33171158C>A , CM000668.2:g.33171158C>A GRCh38
NC_000006.11:g.33138935C>A , CM000668.1:g.33138935C>A GRCh37
NC_000006.10:g.33246913C>A NCBI36
NG_011589.1:g.26311G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000341947.7:c.3322G>T MANE Select ENSP00000339915.2:p.Gly1108Ter
ENST00000341947.6:c.3322G>T ENSP00000339915.2:p.Gly1108Ter
ENST00000361917.5:c.3001G>T ENSP00000355123.1:p.Gly1001Ter
ENST00000374708.8:c.3064G>T ENSP00000363840.4:p.Gly1022Ter
ENST00000477772.1:n.273-5342G>T
NM_080679.2:c.3001G>T NP_542410.2:p.Gly1001Ter
NM_080680.2:c.3322G>T NP_542411.2:p.Gly1108Ter
NM_080681.2:c.3064G>T NP_542412.2:p.Gly1022Ter
XM_011514298.1:c.2476G>T XP_011512600.1:p.Gly826Ter
XM_011514299.1:c.2608G>T XP_011512601.1:p.Gly870Ter
XM_011514300.1:c.2428G>T XP_011512602.1:p.Gly810Ter
XM_011514301.1:c.2365G>T XP_011512603.1:p.Gly789Ter
XM_011514302.1:c.2209G>T XP_011512604.1:p.Gly737Ter
XM_011514299.2:c.2608G>T XP_011512601.1:p.Gly870Ter
XM_011514300.2:c.2428G>T XP_011512602.1:p.Gly810Ter
XM_011514302.2:c.2209G>T XP_011512604.1:p.Gly737Ter
XM_017010250.1:c.3322G>T XP_016865739.1:p.Gly1108Ter
XM_017010251.2:c.2140G>T XP_016865740.1:p.Gly714Ter
NM_080680.3:c.3322G>T MANE Select NP_542411.2:p.Gly1108Ter
NM_080681.3:c.3064G>T NP_542412.2:p.Gly1022Ter
NM_080679.3:c.3001G>T NP_542410.2:p.Gly1001Ter