Canonical Allele Identifier: CA2678226400

Gene: COL11A2

Linked Data

• gnomAD v4: 6-33164504-GGGGAGAGAGAGGGCTGGCCTCAGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164511_33164534del , CM000668.2:g.33164511_33164534del	GRCh38
NC_000006.11:g.33132288_33132311del , CM000668.1:g.33132288_33132311del	GRCh37
NC_000006.10:g.33240266_33240289del	NCBI36
NG_011589.1:g.32941_32964del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.670-55_670-32del
ENST00000341947.7:c.4864-55_4864-32del MANE Select	ENSP00000339915.2:n.4864-55_4864-32del
ENST00000341947.6:c.4864-55_4864-32del	ENSP00000339915.2:n.4864-55_4864-32del
ENST00000361917.5:c.4543-55_4543-32del	ENSP00000355123.1:n.4543-55_4543-32del
ENST00000374708.8:c.4606-55_4606-32del	ENSP00000363840.4:n.4606-55_4606-32del
ENST00000477772.1:n.654-55_654-32del
NM_080679.2:c.4543-55_4543-32del	NP_542410.2:n.4543-55_4543-32del
NM_080680.2:c.4864-55_4864-32del	NP_542411.2:n.4864-55_4864-32del
NM_080681.2:c.4606-55_4606-32del	NP_542412.2:n.4606-55_4606-32del
XM_011514298.1:c.4018-55_4018-32del	XP_011512600.1:n.4018-55_4018-32del
XM_011514299.1:c.4150-55_4150-32del	XP_011512601.1:n.4150-55_4150-32del
XM_011514300.1:c.3970-55_3970-32del	XP_011512602.1:n.3970-55_3970-32del
XM_011514301.1:c.3907-55_3907-32del	XP_011512603.1:n.3907-55_3907-32del
XM_011514302.1:c.3751-55_3751-32del	XP_011512604.1:n.3751-55_3751-32del
XM_011514299.2:c.4150-55_4150-32del	XP_011512601.1:n.4150-55_4150-32del
XM_011514300.2:c.3970-55_3970-32del	XP_011512602.1:n.3970-55_3970-32del
XM_011514302.2:c.3751-55_3751-32del	XP_011512604.1:n.3751-55_3751-32del
XM_017010250.1:c.4864-55_4864-32del	XP_016865739.1:n.4864-55_4864-32del
XM_017010251.2:c.3682-55_3682-32del	XP_016865740.1:n.3682-55_3682-32del
NM_080680.3:c.4864-55_4864-32del MANE Select	NP_542411.2:n.4864-55_4864-32del
NM_080681.3:c.4606-55_4606-32del	NP_542412.2:n.4606-55_4606-32del
NM_080679.3:c.4543-55_4543-32del	NP_542410.2:n.4543-55_4543-32del