Canonical Allele Identifier: CA2034476602

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47977814_47977817delinsAAGC , CM000674.2:g.47977814_47977817delinsAAGC	GRCh38
NC_000012.11:g.48371597_48371600delinsAAGC , CM000674.1:g.48371597_48371600delinsAAGC	GRCh37
NC_000012.10:g.46657864_46657867delinsAAGC	NCBI36
NG_008072.1:g.31686_31689delinsGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.2905-164_2905-161delinsGCTT	ENSP00000338213.6:n.2905-164_2905-161delinsGCTT
ENST00000380518.8:c.3112-164_3112-161delinsGCTT MANE Select	ENSP00000369889.3:n.3112-164_3112-161delinsGCTT
ENST00000337299.6:c.2905-164_2905-161delinsGCTT	ENSP00000338213.6:n.2905-164_2905-161delinsGCTT
ENST00000380518.7:c.3112-164_3112-161delinsGCTT	ENSP00000369889.3:n.3112-164_3112-161delinsGCTT
ENST00000493991.5:n.2198-164_2198-161delinsGCTT
NM_001844.4:c.3112-164_3112-161delinsGCTT	NP_001835.3:n.3112-164_3112-161delinsGCTT
NM_033150.2:c.2905-164_2905-161delinsGCTT	NP_149162.2:n.2905-164_2905-161delinsGCTT
XM_006719242.2:c.3256-164_3256-161delinsGCTT	XP_006719305.2:n.3256-164_3256-161delinsGCTT
XM_011537928.1:c.3256-164_3256-161delinsGCTT	XP_011536230.1:n.3256-164_3256-161delinsGCTT
XM_011537929.1:c.3256-164_3256-161delinsGCTT	XP_011536231.1:n.3256-164_3256-161delinsGCTT
XM_011537930.1:c.3256-164_3256-161delinsGCTT	XP_011536232.1:n.3256-164_3256-161delinsGCTT
XM_011537931.1:c.3256-164_3256-161delinsGCTT	XP_011536233.1:n.3256-164_3256-161delinsGCTT
XM_011537932.1:c.3256-164_3256-161delinsGCTT	XP_011536234.1:n.3256-164_3256-161delinsGCTT
XM_011537933.1:c.3256-164_3256-161delinsGCTT	XP_011536235.1:n.3256-164_3256-161delinsGCTT
XM_011537934.1:c.3253-164_3253-161delinsGCTT	XP_011536236.1:n.3253-164_3253-161delinsGCTT
XM_011537935.1:c.2200-164_2200-161delinsGCTT	XP_011536237.1:n.2200-164_2200-161delinsGCTT
XM_017018828.1:c.3256-164_3256-161delinsGCTT	XP_016874317.1:n.3256-164_3256-161delinsGCTT
XM_017018829.1:c.3253-164_3253-161delinsGCTT	XP_016874318.1:n.3253-164_3253-161delinsGCTT
XM_017018830.1:c.3046-164_3046-161delinsGCTT	XP_016874319.1:n.3046-164_3046-161delinsGCTT
XM_017018831.2:c.2566-164_2566-161delinsGCTT	XP_016874320.1:n.2566-164_2566-161delinsGCTT
NM_001844.5:c.3112-164_3112-161delinsGCTT MANE Select	NP_001835.3:n.3112-164_3112-161delinsGCTT
NM_033150.3:c.2905-164_2905-161delinsGCTT	NP_149162.2:n.2905-164_2905-161delinsGCTT