Canonical Allele Identifier: CA137064372

Gene: COL11A2

Linked Data

• dbSNP Id: rs34657627
• MyVariant Identifiers: chr6:g.33137405_33137406insG (hg19) ; chr6:g.33169628_33169629insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33169632dup , CM000668.2:g.33169632dup	GRCh38
NC_000006.11:g.33137409dup , CM000668.1:g.33137409dup	GRCh37
NC_000006.10:g.33245387dup	NCBI36
NG_011589.1:g.27840dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341947.7:c.3691-139dup MANE Select	ENSP00000339915.2:n.3691-139dup
ENST00000341947.6:c.3691-139dup	ENSP00000339915.2:n.3691-139dup
ENST00000361917.5:c.3370-139dup	ENSP00000355123.1:n.3370-139dup
ENST00000374708.8:c.3433-139dup	ENSP00000363840.4:n.3433-139dup
ENST00000477772.1:n.273-3813dup
NM_080679.2:c.3370-139dup	NP_542410.2:n.3370-139dup
NM_080680.2:c.3691-139dup	NP_542411.2:n.3691-139dup
NM_080681.2:c.3433-139dup	NP_542412.2:n.3433-139dup
XM_011514298.1:c.2845-139dup	XP_011512600.1:n.2845-139dup
XM_011514299.1:c.2977-139dup	XP_011512601.1:n.2977-139dup
XM_011514300.1:c.2797-139dup	XP_011512602.1:n.2797-139dup
XM_011514301.1:c.2734-139dup	XP_011512603.1:n.2734-139dup
XM_011514302.1:c.2578-139dup	XP_011512604.1:n.2578-139dup
XM_011514299.2:c.2977-139dup	XP_011512601.1:n.2977-139dup
XM_011514300.2:c.2797-139dup	XP_011512602.1:n.2797-139dup
XM_011514302.2:c.2578-139dup	XP_011512604.1:n.2578-139dup
XM_017010250.1:c.3691-139dup	XP_016865739.1:n.3691-139dup
XM_017010251.2:c.2509-139dup	XP_016865740.1:n.2509-139dup
NM_080680.3:c.3691-139dup MANE Select	NP_542411.2:n.3691-139dup
NM_080681.3:c.3433-139dup	NP_542412.2:n.3433-139dup
NM_080679.3:c.3370-139dup	NP_542410.2:n.3370-139dup