Canonical Allele Identifier: CA1347589181

Gene: COLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470447T= , CM000665.2:g.15470447T=	GRCh38
NC_000003.11:g.15511954T= , CM000665.1:g.15511954T=	GRCh37
NC_000003.10:g.15486958T=	NCBI36
NG_009032.1:g.56305A=
NG_009032.2:g.56305A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.717+89A= MANE Select	ENSP00000373298.3:n.717+89A=
ENST00000604401.2:n.713+89A=
ENST00000679838.1:c.*479+89A=	ENSP00000505708.1:n.*479+89A=
ENST00000680545.1:n.483+89A=
ENST00000681097.1:c.717+89A=	ENSP00000505397.1:n.717+89A=
ENST00000383781.8:c.687+89A=	ENSP00000373291.3:n.687+89A=
ENST00000383786.9:c.615+89A=	ENSP00000373296.3:n.615+89A=
ENST00000383788.9:c.717+89A=	ENSP00000373298.3:n.717+89A=
ENST00000603808.5:c.717+89A=	ENSP00000474271.1:n.717+89A=
ENST00000605797.1:c.546+89A=	ENSP00000474936.1:n.546+89A=
NM_005677.3:c.717+89A=	NP_005668.2:n.717+89A=
NM_080538.2:c.687+89A=	NP_536799.1:n.687+89A=
NM_080539.3:c.615+89A=	NP_536800.2:n.615+89A=
NM_005677.4:c.717+89A= MANE Select	NP_005668.2:n.717+89A=
NM_080539.4:c.615+89A=	NP_536800.2:n.615+89A=