Canonical Allele Identifier: CA2244609539

Gene: MINK1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4897733G= , CM000679.2:g.4897733G=	GRCh38
NC_000017.10:g.4801028G= , CM000679.1:g.4801028G=	GRCh37
NC_000017.9:g.4741804G=	NCBI36
NG_008029.2:g.10343C=
NG_028005.1:g.69394G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355280.11:c.*446G= MANE Select	ENSP00000347427.6:n.*446G=
ENST00000347992.11:c.*446G=	ENSP00000269296.7:n.*446G=
ENST00000355280.10:c.*446G=	ENSP00000347427.6:n.*446G=
ENST00000571207.5:c.4241G=
ENST00000572330.5:n.5227G=
ENST00000574453.5:c.*4114G=	ENSP00000461500.1:n.*4114G=
ENST00000574871.1:n.2823G=
NM_001024937.3:c.*446G=	NP_001020108.1:n.*446G=
NM_015716.4:c.*446G=	NP_056531.1:n.*446G=
NM_153827.4:c.*446G=	NP_722549.2:n.*446G=
NM_170663.4:c.*446G=	NP_733763.1:n.*446G=
XM_005256664.2:c.*446G=	XP_005256721.1:n.*446G=
XM_005256665.2:c.*446G=	XP_005256722.1:n.*446G=
XM_006721530.2:c.*446G=	XP_006721593.1:n.*446G=
XM_006721531.2:c.*446G=	XP_006721594.1:n.*446G=
XM_006721532.2:c.*446G=	XP_006721595.1:n.*446G=
XM_006721533.2:c.*446G=	XP_006721596.1:n.*446G=
XM_006721534.2:c.*446G=	XP_006721597.1:n.*446G=
XM_006721535.2:c.*446G=	XP_006721598.1:n.*446G=
XM_006721536.2:c.*446G=	XP_006721599.1:n.*446G=
XM_006721538.2:c.*446G=	XP_006721601.1:n.*446G=
XM_011523905.1:c.*446G=	XP_011522207.1:n.*446G=
XM_011523906.1:c.*446G=	XP_011522208.1:n.*446G=
XM_011523907.1:c.*446G=	XP_011522209.1:n.*446G=
XM_011523908.1:c.*446G=	XP_011522210.1:n.*446G=
NM_001321236.1:c.*446G=	NP_001308165.1:n.*446G=
XM_017024704.1:c.*446G=	XP_016880193.1:n.*446G=
XM_017024705.1:c.*446G=	XP_016880194.1:n.*446G=
XM_017024706.1:c.*446G=	XP_016880195.1:n.*446G=
XM_017024707.2:c.*446G=	XP_016880196.1:n.*446G=
XM_017024708.1:c.*446G=	XP_016880197.1:n.*446G=
XR_001752522.2:n.4790G=
NM_153827.5:c.*446G= MANE Select	NP_722549.2:n.*446G=
NM_001024937.4:c.*446G=	NP_001020108.1:n.*446G=
NM_001321236.2:c.*446G=	NP_001308165.1:n.*446G=
NM_015716.5:c.*446G=	NP_056531.1:n.*446G=
NM_170663.5:c.*446G=	NP_733763.1:n.*446G=