Canonical Allele Identifier: CA974318
Gene: COL11A1 HGNC NCBI

Linked Data

dbSNP Id: rs760985656

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.102978820dup , CM000663.2:g.102978820dup GRCh38
NC_000001.10:g.103444376dup , CM000663.1:g.103444376dup GRCh37
NC_000001.9:g.103216964dup NCBI36
NG_008033.1:g.134684dup
NG_008033.2:g.134684dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.2709+47dup MANE Select ENSP00000359114.3:n.2709+47dup
ENST00000353414.8:c.2592+47dup ENSP00000302551.6:n.2592+47dup
ENST00000358392.6:c.2745+47dup ENSP00000351163.2:n.2745+47dup
ENST00000370096.7:c.2709+47dup ENSP00000359114.3:n.2709+47dup
ENST00000512756.5:c.2361+47dup ENSP00000426533.1:n.2361+47dup
ENST00000635193.1:c.2043+47dup
NM_001190709.1:c.2592+47dup NP_001177638.1:n.2592+47dup
NM_001854.3:c.2709+47dup NP_001845.3:n.2709+47dup
NM_080629.2:c.2745+47dup NP_542196.2:n.2745+47dup
NM_080630.3:c.2361+47dup NP_542197.3:n.2361+47dup
XM_011540719.1:c.2709+47dup XP_011539021.1:n.2709+47dup
XM_011540720.1:c.942+47dup XP_011539022.1:n.942+47dup
XM_011540721.1:c.297+47dup XP_011539023.1:n.297+47dup
XR_946545.1:n.3123+47dup
NR_134980.1:n.3043+47dup
XM_017000334.1:c.2862+47dup XP_016855823.1:n.2862+47dup
XM_017000335.1:c.2856+47dup XP_016855824.1:n.2856+47dup
XM_017000336.1:c.2862+47dup XP_016855825.1:n.2862+47dup
XM_017000337.1:c.1260+47dup XP_016855826.1:n.1260+47dup
NM_001854.4:c.2709+47dup MANE Select NP_001845.3:n.2709+47dup
NM_080630.4:c.2361+47dup NP_542197.3:n.2361+47dup
NR_134980.2:n.3069+47dup
NM_001190709.2:c.2592+47dup NP_001177638.1:n.2592+47dup
NM_080629.3:c.2745+47dup NP_542196.2:n.2745+47dup