Canonical Allele Identifier: CA772621572

Gene: MINK1

Linked Data

• dbSNP Id: rs1258612410
• gnomAD v3: 17-4897762-ATTTC-A
• gnomAD v4: 17-4897762-ATTTC-A
• MyVariant Identifiers: chr17:g.4801058_4801061del (hg19) ; chr17:g.4897763_4897766del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4897765_4897768del , CM000679.2:g.4897765_4897768del	GRCh38
NC_000017.10:g.4801060_4801063del , CM000679.1:g.4801060_4801063del	GRCh37
NC_000017.9:g.4741836_4741839del	NCBI36
NG_008029.2:g.10310_10313del
NG_028005.1:g.69426_69429del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355280.11:c.*478_*481del MANE Select	ENSP00000347427.6:n.*478_*481del
ENST00000347992.11:c.*478_*481del	ENSP00000269296.7:n.*478_*481del
ENST00000355280.10:c.*478_*481del	ENSP00000347427.6:n.*478_*481del
ENST00000571207.5:c.4273_4276del
ENST00000572330.5:n.5259_5262del
ENST00000574453.5:c.*4146_*4149del	ENSP00000461500.1:n.*4146_*4149del
ENST00000574871.1:n.2855_2858del
NM_001024937.3:c.*478_*481del	NP_001020108.1:n.*478_*481del
NM_015716.4:c.*478_*481del	NP_056531.1:n.*478_*481del
NM_153827.4:c.*478_*481del	NP_722549.2:n.*478_*481del
NM_170663.4:c.*478_*481del	NP_733763.1:n.*478_*481del
XM_005256664.2:c.*478_*481del	XP_005256721.1:n.*478_*481del
XM_005256665.2:c.*478_*481del	XP_005256722.1:n.*478_*481del
XM_006721530.2:c.*478_*481del	XP_006721593.1:n.*478_*481del
XM_006721531.2:c.*478_*481del	XP_006721594.1:n.*478_*481del
XM_006721532.2:c.*478_*481del	XP_006721595.1:n.*478_*481del
XM_006721533.2:c.*478_*481del	XP_006721596.1:n.*478_*481del
XM_006721534.2:c.*478_*481del	XP_006721597.1:n.*478_*481del
XM_006721535.2:c.*478_*481del	XP_006721598.1:n.*478_*481del
XM_006721536.2:c.*478_*481del	XP_006721599.1:n.*478_*481del
XM_006721538.2:c.*478_*481del	XP_006721601.1:n.*478_*481del
XM_011523905.1:c.*478_*481del	XP_011522207.1:n.*478_*481del
XM_011523906.1:c.*478_*481del	XP_011522208.1:n.*478_*481del
XM_011523907.1:c.*478_*481del	XP_011522209.1:n.*478_*481del
XM_011523908.1:c.*478_*481del	XP_011522210.1:n.*478_*481del
NM_001321236.1:c.*478_*481del	NP_001308165.1:n.*478_*481del
XM_017024704.1:c.*478_*481del	XP_016880193.1:n.*478_*481del
XM_017024705.1:c.*478_*481del	XP_016880194.1:n.*478_*481del
XM_017024706.1:c.*478_*481del	XP_016880195.1:n.*478_*481del
XM_017024707.2:c.*478_*481del	XP_016880196.1:n.*478_*481del
XM_017024708.1:c.*478_*481del	XP_016880197.1:n.*478_*481del
XR_001752522.2:n.4822_4825del
NM_153827.5:c.*478_*481del MANE Select	NP_722549.2:n.*478_*481del
NM_001024937.4:c.*478_*481del	NP_001020108.1:n.*478_*481del
NM_001321236.2:c.*478_*481del	NP_001308165.1:n.*478_*481del
NM_015716.5:c.*478_*481del	NP_056531.1:n.*478_*481del
NM_170663.5:c.*478_*481del	NP_733763.1:n.*478_*481del