Canonical Allele Identifier: CA1619890508

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164903G= , CM000668.2:g.33164903G=	GRCh38
NC_000006.11:g.33132680G= , CM000668.1:g.33132680G=	GRCh37
NC_000006.10:g.33240658G=	NCBI36
NG_011589.1:g.32566C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.618C=
ENST00000341947.7:c.4812C= MANE Select	ENSP00000339915.2:p.Asn1604=
ENST00000341947.6:c.4812C=	ENSP00000339915.2:p.Asn1604=
ENST00000361917.5:c.4491C=	ENSP00000355123.1:p.Asn1497=
ENST00000374708.8:c.4554C=	ENSP00000363840.4:p.Asn1518=
ENST00000477772.1:n.602C=
NM_080679.2:c.4491C=	NP_542410.2:p.Asn1497=
NM_080680.2:c.4812C=	NP_542411.2:p.Asn1604=
NM_080681.2:c.4554C=	NP_542412.2:p.Asn1518=
XM_011514298.1:c.3966C=	XP_011512600.1:p.Asn1322=
XM_011514299.1:c.4098C=	XP_011512601.1:p.Asn1366=
XM_011514300.1:c.3918C=	XP_011512602.1:p.Asn1306=
XM_011514301.1:c.3855C=	XP_011512603.1:p.Asn1285=
XM_011514302.1:c.3699C=	XP_011512604.1:p.Asn1233=
XM_011514299.2:c.4098C=	XP_011512601.1:p.Asn1366=
XM_011514300.2:c.3918C=	XP_011512602.1:p.Asn1306=
XM_011514302.2:c.3699C=	XP_011512604.1:p.Asn1233=
XM_017010250.1:c.4812C=	XP_016865739.1:p.Asn1604=
XM_017010251.2:c.3630C=	XP_016865740.1:p.Asn1210=
NM_080680.3:c.4812C= MANE Select	NP_542411.2:p.Asn1604=
NM_080681.3:c.4554C=	NP_542412.2:p.Asn1518=
NM_080679.3:c.4491C=	NP_542410.2:p.Asn1497=