Canonical Allele Identifier: CA1619890404
Gene: COL11A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33164855C= , CM000668.2:g.33164855C= GRCh38
NC_000006.11:g.33132632C= , CM000668.1:g.33132632C= GRCh37
NC_000006.10:g.33240610C= NCBI36
NG_011589.1:g.32614G=

Transcript Alleles

HGVS Amino-acid change
ENST00000683572.1:n.666G=
ENST00000341947.7:c.4860G= MANE Select ENSP00000339915.2:p.Thr1620=
ENST00000341947.6:c.4860G= ENSP00000339915.2:p.Thr1620=
ENST00000361917.5:c.4539G= ENSP00000355123.1:p.Thr1513=
ENST00000374708.8:c.4602G= ENSP00000363840.4:p.Thr1534=
ENST00000477772.1:n.650G=
NM_080679.2:c.4539G= NP_542410.2:p.Thr1513=
NM_080680.2:c.4860G= NP_542411.2:p.Thr1620=
NM_080681.2:c.4602G= NP_542412.2:p.Thr1534=
XM_011514298.1:c.4014G= XP_011512600.1:p.Thr1338=
XM_011514299.1:c.4146G= XP_011512601.1:p.Thr1382=
XM_011514300.1:c.3966G= XP_011512602.1:p.Thr1322=
XM_011514301.1:c.3903G= XP_011512603.1:p.Thr1301=
XM_011514302.1:c.3747G= XP_011512604.1:p.Thr1249=
XM_011514299.2:c.4146G= XP_011512601.1:p.Thr1382=
XM_011514300.2:c.3966G= XP_011512602.1:p.Thr1322=
XM_011514302.2:c.3747G= XP_011512604.1:p.Thr1249=
XM_017010250.1:c.4860G= XP_016865739.1:p.Thr1620=
XM_017010251.2:c.3678G= XP_016865740.1:p.Thr1226=
NM_080680.3:c.4860G= MANE Select NP_542411.2:p.Thr1620=
NM_080681.3:c.4602G= NP_542412.2:p.Thr1534=
NM_080679.3:c.4539G= NP_542410.2:p.Thr1513=