Canonical Allele Identifier: CA1619890454

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164875T= , CM000668.2:g.33164875T=	GRCh38
NC_000006.11:g.33132652T= , CM000668.1:g.33132652T=	GRCh37
NC_000006.10:g.33240630T=	NCBI36
NG_011589.1:g.32594A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.646A=
ENST00000341947.7:c.4840A= MANE Select	ENSP00000339915.2:p.Thr1614=
ENST00000341947.6:c.4840A=	ENSP00000339915.2:p.Thr1614=
ENST00000361917.5:c.4519A=	ENSP00000355123.1:p.Thr1507=
ENST00000374708.8:c.4582A=	ENSP00000363840.4:p.Thr1528=
ENST00000477772.1:n.630A=
NM_080679.2:c.4519A=	NP_542410.2:p.Thr1507=
NM_080680.2:c.4840A=	NP_542411.2:p.Thr1614=
NM_080681.2:c.4582A=	NP_542412.2:p.Thr1528=
XM_011514298.1:c.3994A=	XP_011512600.1:p.Thr1332=
XM_011514299.1:c.4126A=	XP_011512601.1:p.Thr1376=
XM_011514300.1:c.3946A=	XP_011512602.1:p.Thr1316=
XM_011514301.1:c.3883A=	XP_011512603.1:p.Thr1295=
XM_011514302.1:c.3727A=	XP_011512604.1:p.Thr1243=
XM_011514299.2:c.4126A=	XP_011512601.1:p.Thr1376=
XM_011514300.2:c.3946A=	XP_011512602.1:p.Thr1316=
XM_011514302.2:c.3727A=	XP_011512604.1:p.Thr1243=
XM_017010250.1:c.4840A=	XP_016865739.1:p.Thr1614=
XM_017010251.2:c.3658A=	XP_016865740.1:p.Thr1220=
NM_080680.3:c.4840A= MANE Select	NP_542411.2:p.Thr1614=
NM_080681.3:c.4582A=	NP_542412.2:p.Thr1528=
NM_080679.3:c.4519A=	NP_542410.2:p.Thr1507=