Canonical Allele Identifier: CA2244609562

Gene: MINK1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4897762_4897771delinsATTTCTTCAT , CM000679.2:g.4897762_4897771delinsATTTCTTCAT	GRCh38
NC_000017.10:g.4801057_4801066delinsATTTCTTCAT , CM000679.1:g.4801057_4801066delinsATTTCTTCAT	GRCh37
NC_000017.9:g.4741833_4741842delinsATTTCTTCAT	NCBI36
NG_008029.2:g.10305_10314delinsATGAAGAAAT
NG_028005.1:g.69423_69432delinsATTTCTTCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355280.11:c.*475_*484delinsATTTCTTCAT MANE Select	ENSP00000347427.6:n.*475_*484delinsATTTCTTCAT
ENST00000347992.11:c.*475_*484delinsATTTCTTCAT	ENSP00000269296.7:n.*475_*484delinsATTTCTTCAT
ENST00000355280.10:c.*475_*484delinsATTTCTTCAT	ENSP00000347427.6:n.*475_*484delinsATTTCTTCAT
ENST00000571207.5:c.4270_4279delinsATTTCTTCAT
ENST00000572330.5:n.5256_5265delinsATTTCTTCAT
ENST00000574453.5:c.*4143_*4152delinsATTTCTTCAT	ENSP00000461500.1:n.*4143_*4152delinsATTTCTTCAT
ENST00000574871.1:n.2852_2861delinsATTTCTTCAT
NM_001024937.3:c.*475_*484delinsATTTCTTCAT	NP_001020108.1:n.*475_*484delinsATTTCTTCAT
NM_015716.4:c.*475_*484delinsATTTCTTCAT	NP_056531.1:n.*475_*484delinsATTTCTTCAT
NM_153827.4:c.*475_*484delinsATTTCTTCAT	NP_722549.2:n.*475_*484delinsATTTCTTCAT
NM_170663.4:c.*475_*484delinsATTTCTTCAT	NP_733763.1:n.*475_*484delinsATTTCTTCAT
XM_005256664.2:c.*475_*484delinsATTTCTTCAT	XP_005256721.1:n.*475_*484delinsATTTCTTCAT
XM_005256665.2:c.*475_*484delinsATTTCTTCAT	XP_005256722.1:n.*475_*484delinsATTTCTTCAT
XM_006721530.2:c.*475_*484delinsATTTCTTCAT	XP_006721593.1:n.*475_*484delinsATTTCTTCAT
XM_006721531.2:c.*475_*484delinsATTTCTTCAT	XP_006721594.1:n.*475_*484delinsATTTCTTCAT
XM_006721532.2:c.*475_*484delinsATTTCTTCAT	XP_006721595.1:n.*475_*484delinsATTTCTTCAT
XM_006721533.2:c.*475_*484delinsATTTCTTCAT	XP_006721596.1:n.*475_*484delinsATTTCTTCAT
XM_006721534.2:c.*475_*484delinsATTTCTTCAT	XP_006721597.1:n.*475_*484delinsATTTCTTCAT
XM_006721535.2:c.*475_*484delinsATTTCTTCAT	XP_006721598.1:n.*475_*484delinsATTTCTTCAT
XM_006721536.2:c.*475_*484delinsATTTCTTCAT	XP_006721599.1:n.*475_*484delinsATTTCTTCAT
XM_006721538.2:c.*475_*484delinsATTTCTTCAT	XP_006721601.1:n.*475_*484delinsATTTCTTCAT
XM_011523905.1:c.*475_*484delinsATTTCTTCAT	XP_011522207.1:n.*475_*484delinsATTTCTTCAT
XM_011523906.1:c.*475_*484delinsATTTCTTCAT	XP_011522208.1:n.*475_*484delinsATTTCTTCAT
XM_011523907.1:c.*475_*484delinsATTTCTTCAT	XP_011522209.1:n.*475_*484delinsATTTCTTCAT
XM_011523908.1:c.*475_*484delinsATTTCTTCAT	XP_011522210.1:n.*475_*484delinsATTTCTTCAT
NM_001321236.1:c.*475_*484delinsATTTCTTCAT	NP_001308165.1:n.*475_*484delinsATTTCTTCAT
XM_017024704.1:c.*475_*484delinsATTTCTTCAT	XP_016880193.1:n.*475_*484delinsATTTCTTCAT
XM_017024705.1:c.*475_*484delinsATTTCTTCAT	XP_016880194.1:n.*475_*484delinsATTTCTTCAT
XM_017024706.1:c.*475_*484delinsATTTCTTCAT	XP_016880195.1:n.*475_*484delinsATTTCTTCAT
XM_017024707.2:c.*475_*484delinsATTTCTTCAT	XP_016880196.1:n.*475_*484delinsATTTCTTCAT
XM_017024708.1:c.*475_*484delinsATTTCTTCAT	XP_016880197.1:n.*475_*484delinsATTTCTTCAT
XR_001752522.2:n.4819_4828delinsATTTCTTCAT
NM_153827.5:c.*475_*484delinsATTTCTTCAT MANE Select	NP_722549.2:n.*475_*484delinsATTTCTTCAT
NM_001024937.4:c.*475_*484delinsATTTCTTCAT	NP_001020108.1:n.*475_*484delinsATTTCTTCAT
NM_001321236.2:c.*475_*484delinsATTTCTTCAT	NP_001308165.1:n.*475_*484delinsATTTCTTCAT
NM_015716.5:c.*475_*484delinsATTTCTTCAT	NP_056531.1:n.*475_*484delinsATTTCTTCAT
NM_170663.5:c.*475_*484delinsATTTCTTCAT	NP_733763.1:n.*475_*484delinsATTTCTTCAT