Canonical Allele Identifier: CA1619905602
Gene: COL11A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33192243C= , CM000668.2:g.33192243C= GRCh38
NC_000006.11:g.33160020C= , CM000668.1:g.33160020C= GRCh37
NC_000006.10:g.33267998C= NCBI36
NG_011589.1:g.5226G=
NG_023374.1:g.13413G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341947.7:c.-3G= MANE Select ENSP00000339915.2:n.-3G=
ENST00000341947.6:c.-3G= ENSP00000339915.2:n.-3G=
ENST00000361917.5:c.-3G= ENSP00000355123.1:n.-3G=
ENST00000374708.8:c.-3G= ENSP00000363840.4:n.-3G=
ENST00000395194.1:c.-3G= ENSP00000378620.1:n.-3G=
ENST00000457788.5:c.-3G= ENSP00000405520.1:n.-3G=
NM_001163771.1:c.-3G= NP_001157243.1:n.-3G=
NM_080679.2:c.-3G= NP_542410.2:n.-3G=
NM_080680.2:c.-3G= NP_542411.2:n.-3G=
NM_080681.2:c.-3G= NP_542412.2:n.-3G=
XM_011514298.1:c.-765+782G= XP_011512600.1:n.-765+782G=
XM_017010250.1:c.-3G= XP_016865739.1:n.-3G=
NM_001163771.2:c.-3G= NP_001157243.1:n.-3G=
NM_080680.3:c.-3G= MANE Select NP_542411.2:n.-3G=
NM_080681.3:c.-3G= NP_542412.2:n.-3G=
NM_080679.3:c.-3G= NP_542410.2:n.-3G=