Canonical Allele Identifier: CA1619890444

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164873C= , CM000668.2:g.33164873C=	GRCh38
NC_000006.11:g.33132650C= , CM000668.1:g.33132650C=	GRCh37
NC_000006.10:g.33240628C=	NCBI36
NG_011589.1:g.32596G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.648G=
ENST00000341947.7:c.4842G= MANE Select	ENSP00000339915.2:p.Thr1614=
ENST00000341947.6:c.4842G=	ENSP00000339915.2:p.Thr1614=
ENST00000361917.5:c.4521G=	ENSP00000355123.1:p.Thr1507=
ENST00000374708.8:c.4584G=	ENSP00000363840.4:p.Thr1528=
ENST00000477772.1:n.632G=
NM_080679.2:c.4521G=	NP_542410.2:p.Thr1507=
NM_080680.2:c.4842G=	NP_542411.2:p.Thr1614=
NM_080681.2:c.4584G=	NP_542412.2:p.Thr1528=
XM_011514298.1:c.3996G=	XP_011512600.1:p.Thr1332=
XM_011514299.1:c.4128G=	XP_011512601.1:p.Thr1376=
XM_011514300.1:c.3948G=	XP_011512602.1:p.Thr1316=
XM_011514301.1:c.3885G=	XP_011512603.1:p.Thr1295=
XM_011514302.1:c.3729G=	XP_011512604.1:p.Thr1243=
XM_011514299.2:c.4128G=	XP_011512601.1:p.Thr1376=
XM_011514300.2:c.3948G=	XP_011512602.1:p.Thr1316=
XM_011514302.2:c.3729G=	XP_011512604.1:p.Thr1243=
XM_017010250.1:c.4842G=	XP_016865739.1:p.Thr1614=
XM_017010251.2:c.3660G=	XP_016865740.1:p.Thr1220=
NM_080680.3:c.4842G= MANE Select	NP_542411.2:p.Thr1614=
NM_080681.3:c.4584G=	NP_542412.2:p.Thr1528=
NM_080679.3:c.4521G=	NP_542410.2:p.Thr1507=