Canonical Allele Identifier: CA363617889
Gene: COL11A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33164957G>T , CM000668.2:g.33164957G>T GRCh38
NC_000006.11:g.33132734G>T , CM000668.1:g.33132734G>T GRCh37
NC_000006.10:g.33240712G>T NCBI36
NG_011589.1:g.32512C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000683572.1:n.564C>A
ENST00000341947.7:c.4758C>A MANE Select ENSP00000339915.2:p.Tyr1586Ter
ENST00000341947.6:c.4758C>A ENSP00000339915.2:p.Tyr1586Ter
ENST00000361917.5:c.4437C>A ENSP00000355123.1:p.Tyr1479Ter
ENST00000374708.8:c.4500C>A ENSP00000363840.4:p.Tyr1500Ter
ENST00000477772.1:n.548C>A
NM_080679.2:c.4437C>A NP_542410.2:p.Tyr1479Ter
NM_080680.2:c.4758C>A NP_542411.2:p.Tyr1586Ter
NM_080681.2:c.4500C>A NP_542412.2:p.Tyr1500Ter
XM_011514298.1:c.3912C>A XP_011512600.1:p.Tyr1304Ter
XM_011514299.1:c.4044C>A XP_011512601.1:p.Tyr1348Ter
XM_011514300.1:c.3864C>A XP_011512602.1:p.Tyr1288Ter
XM_011514301.1:c.3801C>A XP_011512603.1:p.Tyr1267Ter
XM_011514302.1:c.3645C>A XP_011512604.1:p.Tyr1215Ter
XM_011514299.2:c.4044C>A XP_011512601.1:p.Tyr1348Ter
XM_011514300.2:c.3864C>A XP_011512602.1:p.Tyr1288Ter
XM_011514302.2:c.3645C>A XP_011512604.1:p.Tyr1215Ter
XM_017010250.1:c.4758C>A XP_016865739.1:p.Tyr1586Ter
XM_017010251.2:c.3576C>A XP_016865740.1:p.Tyr1192Ter
NM_080680.3:c.4758C>A MANE Select NP_542411.2:p.Tyr1586Ter
NM_080681.3:c.4500C>A NP_542412.2:p.Tyr1500Ter
NM_080679.3:c.4437C>A NP_542410.2:p.Tyr1479Ter