Canonical Allele Identifier: CA1619905648

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33192340A= , CM000668.2:g.33192340A=	GRCh38
NC_000006.11:g.33160117A= , CM000668.1:g.33160117A=	GRCh37
NC_000006.10:g.33268095A=	NCBI36
NG_011589.1:g.5129T=
NG_023374.1:g.13316T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000341947.7:c.-100T= MANE Select	ENSP00000339915.2:n.-100T=
ENST00000341947.6:c.-100T=	ENSP00000339915.2:n.-100T=
ENST00000361917.5:c.-100T=	ENSP00000355123.1:n.-100T=
ENST00000374708.8:c.-100T=	ENSP00000363840.4:n.-100T=
ENST00000395194.1:c.-100T=	ENSP00000378620.1:n.-100T=
ENST00000457788.5:c.-100T=	ENSP00000405520.1:n.-100T=
NM_001163771.1:c.-100T=	NP_001157243.1:n.-100T=
NM_080679.2:c.-100T=	NP_542410.2:n.-100T=
NM_080680.2:c.-100T=	NP_542411.2:n.-100T=
NM_080681.2:c.-100T=	NP_542412.2:n.-100T=
XM_011514298.1:c.-765+685T=	XP_011512600.1:n.-765+685T=
XM_017010250.1:c.-66-34T=	XP_016865739.1:n.-66-34T=
NM_001163771.2:c.-100T=	NP_001157243.1:n.-100T=
NM_080680.3:c.-100T= MANE Select	NP_542411.2:n.-100T=
NM_080681.3:c.-100T=	NP_542412.2:n.-100T=
NM_080679.3:c.-100T=	NP_542410.2:n.-100T=