Canonical Allele Identifier: CA1619905600

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33192239A= , CM000668.2:g.33192239A=	GRCh38
NC_000006.11:g.33160016A= , CM000668.1:g.33160016A=	GRCh37
NC_000006.10:g.33267994A=	NCBI36
NG_011589.1:g.5230T=
NG_023374.1:g.13417T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341947.7:c.2T= MANE Select	ENSP00000339915.2:p.Met1=
ENST00000341947.6:c.2T=	ENSP00000339915.2:p.Met1=
ENST00000361917.5:c.2T=	ENSP00000355123.1:p.Met1=
ENST00000374708.8:c.2T=	ENSP00000363840.4:p.Met1=
ENST00000395194.1:c.2T=	ENSP00000378620.1:p.Met1=
ENST00000457788.5:c.2T=	ENSP00000405520.1:p.Met1=
NM_001163771.1:c.2T=	NP_001157243.1:p.Met1=
NM_080679.2:c.2T=	NP_542410.2:p.Met1=
NM_080680.2:c.2T=	NP_542411.2:p.Met1=
NM_080681.2:c.2T=	NP_542412.2:p.Met1=
XM_011514298.1:c.-765+786T=	XP_011512600.1:n.-765+786T=
XM_017010250.1:c.2T=	XP_016865739.1:p.Met1=
NM_001163771.2:c.2T=	NP_001157243.1:p.Met1=
NM_080680.3:c.2T= MANE Select	NP_542411.2:p.Met1=
NM_080681.3:c.2T=	NP_542412.2:p.Met1=
NM_080679.3:c.2T=	NP_542410.2:p.Met1=