Canonical Allele Identifier: CA1619905647

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33192336C= , CM000668.2:g.33192336C=	GRCh38
NC_000006.11:g.33160113C= , CM000668.1:g.33160113C=	GRCh37
NC_000006.10:g.33268091C=	NCBI36
NG_011589.1:g.5133G=
NG_023374.1:g.13320G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000341947.7:c.-96G= MANE Select	ENSP00000339915.2:n.-96G=
ENST00000341947.6:c.-96G=	ENSP00000339915.2:n.-96G=
ENST00000361917.5:c.-96G=	ENSP00000355123.1:n.-96G=
ENST00000374708.8:c.-96G=	ENSP00000363840.4:n.-96G=
ENST00000395194.1:c.-96G=	ENSP00000378620.1:n.-96G=
ENST00000457788.5:c.-96G=	ENSP00000405520.1:n.-96G=
NM_001163771.1:c.-96G=	NP_001157243.1:n.-96G=
NM_080679.2:c.-96G=	NP_542410.2:n.-96G=
NM_080680.2:c.-96G=	NP_542411.2:n.-96G=
NM_080681.2:c.-96G=	NP_542412.2:n.-96G=
XM_011514298.1:c.-765+689G=	XP_011512600.1:n.-765+689G=
XM_017010250.1:c.-66-30G=	XP_016865739.1:n.-66-30G=
NM_001163771.2:c.-96G=	NP_001157243.1:n.-96G=
NM_080680.3:c.-96G= MANE Select	NP_542411.2:n.-96G=
NM_080681.3:c.-96G=	NP_542412.2:n.-96G=
NM_080679.3:c.-96G=	NP_542410.2:n.-96G=