Canonical Allele Identifier: CA1619889829

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164429C= , CM000668.2:g.33164429C=	GRCh38
NC_000006.11:g.33132206C= , CM000668.1:g.33132206C=	GRCh37
NC_000006.10:g.33240184C=	NCBI36
NG_011589.1:g.33040G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.714G=
ENST00000341947.7:c.4908G= MANE Select	ENSP00000339915.2:p.Gln1636=
ENST00000341947.6:c.4908G=	ENSP00000339915.2:p.Gln1636=
ENST00000361917.5:c.4587G=	ENSP00000355123.1:p.Gln1529=
ENST00000374708.8:c.4650G=	ENSP00000363840.4:p.Gln1550=
ENST00000477772.1:n.698G=
NM_080679.2:c.4587G=	NP_542410.2:p.Gln1529=
NM_080680.2:c.4908G=	NP_542411.2:p.Gln1636=
NM_080681.2:c.4650G=	NP_542412.2:p.Gln1550=
XM_011514298.1:c.4062G=	XP_011512600.1:p.Gln1354=
XM_011514299.1:c.4194G=	XP_011512601.1:p.Gln1398=
XM_011514300.1:c.4014G=	XP_011512602.1:p.Gln1338=
XM_011514301.1:c.3951G=	XP_011512603.1:p.Gln1317=
XM_011514302.1:c.3795G=	XP_011512604.1:p.Gln1265=
XM_011514299.2:c.4194G=	XP_011512601.1:p.Gln1398=
XM_011514300.2:c.4014G=	XP_011512602.1:p.Gln1338=
XM_011514302.2:c.3795G=	XP_011512604.1:p.Gln1265=
XM_017010250.1:c.4908G=	XP_016865739.1:p.Gln1636=
XM_017010251.2:c.3726G=	XP_016865740.1:p.Gln1242=
NM_080680.3:c.4908G= MANE Select	NP_542411.2:p.Gln1636=
NM_080681.3:c.4650G=	NP_542412.2:p.Gln1550=
NM_080679.3:c.4587G=	NP_542410.2:p.Gln1529=