Canonical Allele Identifier: CA1619890827

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33165130_33165146delinsACTGCAGCATCCTACTG , CM000668.2:g.33165130_33165146delinsACTGCAGCATCCTACTG	GRCh38
NC_000006.11:g.33132907_33132923delinsACTGCAGCATCCTACTG , CM000668.1:g.33132907_33132923delinsACTGCAGCATCCTACTG	GRCh37
NC_000006.10:g.33240885_33240901delinsACTGCAGCATCCTACTG	NCBI36
NG_011589.1:g.32323_32339delinsCAGTAGGATGCTGCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.557-182_557-166delinsCAGTAGGATGCTGCAGT
ENST00000341947.7:c.4751-182_4751-166delinsCAGTAGGATGCTGCAGT MANE Select	ENSP00000339915.2:n.4751-182_4751-166delinsCAGTAGGATGCTGCAGT
ENST00000341947.6:c.4751-182_4751-166delinsCAGTAGGATGCTGCAGT	ENSP00000339915.2:n.4751-182_4751-166delinsCAGTAGGATGCTGCAGT
ENST00000361917.5:c.4430-182_4430-166delinsCAGTAGGATGCTGCAGT	ENSP00000355123.1:n.4430-182_4430-166delinsCAGTAGGATGCTGCAGT
ENST00000374708.8:c.4493-182_4493-166delinsCAGTAGGATGCTGCAGT	ENSP00000363840.4:n.4493-182_4493-166delinsCAGTAGGATGCTGCAGT
ENST00000477772.1:n.541-182_541-166delinsCAGTAGGATGCTGCAGT
NM_080679.2:c.4430-182_4430-166delinsCAGTAGGATGCTGCAGT	NP_542410.2:n.4430-182_4430-166delinsCAGTAGGATGCTGCAGT
NM_080680.2:c.4751-182_4751-166delinsCAGTAGGATGCTGCAGT	NP_542411.2:n.4751-182_4751-166delinsCAGTAGGATGCTGCAGT
NM_080681.2:c.4493-182_4493-166delinsCAGTAGGATGCTGCAGT	NP_542412.2:n.4493-182_4493-166delinsCAGTAGGATGCTGCAGT
XM_011514298.1:c.3905-182_3905-166delinsCAGTAGGATGCTGCAGT	XP_011512600.1:n.3905-182_3905-166delinsCAGTAGGATGCTGCAGT
XM_011514299.1:c.4037-182_4037-166delinsCAGTAGGATGCTGCAGT	XP_011512601.1:n.4037-182_4037-166delinsCAGTAGGATGCTGCAGT
XM_011514300.1:c.3857-182_3857-166delinsCAGTAGGATGCTGCAGT	XP_011512602.1:n.3857-182_3857-166delinsCAGTAGGATGCTGCAGT
XM_011514301.1:c.3794-182_3794-166delinsCAGTAGGATGCTGCAGT	XP_011512603.1:n.3794-182_3794-166delinsCAGTAGGATGCTGCAGT
XM_011514302.1:c.3638-182_3638-166delinsCAGTAGGATGCTGCAGT	XP_011512604.1:n.3638-182_3638-166delinsCAGTAGGATGCTGCAGT
XM_011514299.2:c.4037-182_4037-166delinsCAGTAGGATGCTGCAGT	XP_011512601.1:n.4037-182_4037-166delinsCAGTAGGATGCTGCAGT
XM_011514300.2:c.3857-182_3857-166delinsCAGTAGGATGCTGCAGT	XP_011512602.1:n.3857-182_3857-166delinsCAGTAGGATGCTGCAGT
XM_011514302.2:c.3638-182_3638-166delinsCAGTAGGATGCTGCAGT	XP_011512604.1:n.3638-182_3638-166delinsCAGTAGGATGCTGCAGT
XM_017010250.1:c.4751-182_4751-166delinsCAGTAGGATGCTGCAGT	XP_016865739.1:n.4751-182_4751-166delinsCAGTAGGATGCTGCAGT
XM_017010251.2:c.3569-182_3569-166delinsCAGTAGGATGCTGCAGT	XP_016865740.1:n.3569-182_3569-166delinsCAGTAGGATGCTGCAGT
NM_080680.3:c.4751-182_4751-166delinsCAGTAGGATGCTGCAGT MANE Select	NP_542411.2:n.4751-182_4751-166delinsCAGTAGGATGCTGCAGT
NM_080681.3:c.4493-182_4493-166delinsCAGTAGGATGCTGCAGT	NP_542412.2:n.4493-182_4493-166delinsCAGTAGGATGCTGCAGT
NM_080679.3:c.4430-182_4430-166delinsCAGTAGGATGCTGCAGT	NP_542410.2:n.4430-182_4430-166delinsCAGTAGGATGCTGCAGT