Canonical Allele Identifier: CA1619890353

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164824_33164834delinsGGAGGGGCAGC , CM000668.2:g.33164824_33164834delinsGGAGGGGCAGC	GRCh38
NC_000006.11:g.33132601_33132611delinsGGAGGGGCAGC , CM000668.1:g.33132601_33132611delinsGGAGGGGCAGC	GRCh37
NC_000006.10:g.33240579_33240589delinsGGAGGGGCAGC	NCBI36
NG_011589.1:g.32635_32645delinsGCTGCCCCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.669+18_669+28delinsGCTGCCCCTCC
ENST00000341947.7:c.4863+18_4863+28delinsGCTGCCCCTCC MANE Select	ENSP00000339915.2:n.4863+18_4863+28delinsGCTGCCCCTCC
ENST00000341947.6:c.4863+18_4863+28delinsGCTGCCCCTCC	ENSP00000339915.2:n.4863+18_4863+28delinsGCTGCCCCTCC
ENST00000361917.5:c.4542+18_4542+28delinsGCTGCCCCTCC	ENSP00000355123.1:n.4542+18_4542+28delinsGCTGCCCCTCC
ENST00000374708.8:c.4605+18_4605+28delinsGCTGCCCCTCC	ENSP00000363840.4:n.4605+18_4605+28delinsGCTGCCCCTCC
ENST00000477772.1:n.653+18_653+28delinsGCTGCCCCTCC
NM_080679.2:c.4542+18_4542+28delinsGCTGCCCCTCC	NP_542410.2:n.4542+18_4542+28delinsGCTGCCCCTCC
NM_080680.2:c.4863+18_4863+28delinsGCTGCCCCTCC	NP_542411.2:n.4863+18_4863+28delinsGCTGCCCCTCC
NM_080681.2:c.4605+18_4605+28delinsGCTGCCCCTCC	NP_542412.2:n.4605+18_4605+28delinsGCTGCCCCTCC
XM_011514298.1:c.4017+18_4017+28delinsGCTGCCCCTCC	XP_011512600.1:n.4017+18_4017+28delinsGCTGCCCCTCC
XM_011514299.1:c.4149+18_4149+28delinsGCTGCCCCTCC	XP_011512601.1:n.4149+18_4149+28delinsGCTGCCCCTCC
XM_011514300.1:c.3969+18_3969+28delinsGCTGCCCCTCC	XP_011512602.1:n.3969+18_3969+28delinsGCTGCCCCTCC
XM_011514301.1:c.3906+18_3906+28delinsGCTGCCCCTCC	XP_011512603.1:n.3906+18_3906+28delinsGCTGCCCCTCC
XM_011514302.1:c.3750+18_3750+28delinsGCTGCCCCTCC	XP_011512604.1:n.3750+18_3750+28delinsGCTGCCCCTCC
XM_011514299.2:c.4149+18_4149+28delinsGCTGCCCCTCC	XP_011512601.1:n.4149+18_4149+28delinsGCTGCCCCTCC
XM_011514300.2:c.3969+18_3969+28delinsGCTGCCCCTCC	XP_011512602.1:n.3969+18_3969+28delinsGCTGCCCCTCC
XM_011514302.2:c.3750+18_3750+28delinsGCTGCCCCTCC	XP_011512604.1:n.3750+18_3750+28delinsGCTGCCCCTCC
XM_017010250.1:c.4863+18_4863+28delinsGCTGCCCCTCC	XP_016865739.1:n.4863+18_4863+28delinsGCTGCCCCTCC
XM_017010251.2:c.3681+18_3681+28delinsGCTGCCCCTCC	XP_016865740.1:n.3681+18_3681+28delinsGCTGCCCCTCC
NM_080680.3:c.4863+18_4863+28delinsGCTGCCCCTCC MANE Select	NP_542411.2:n.4863+18_4863+28delinsGCTGCCCCTCC
NM_080681.3:c.4605+18_4605+28delinsGCTGCCCCTCC	NP_542412.2:n.4605+18_4605+28delinsGCTGCCCCTCC
NM_080679.3:c.4542+18_4542+28delinsGCTGCCCCTCC	NP_542410.2:n.4542+18_4542+28delinsGCTGCCCCTCC