Canonical Allele Identifier: CA2635575837

Gene: MINK1 CHRNE

Linked Data

• gnomAD v4: 17-4897978-T-TCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4897979_4897980insACC , CM000679.2:g.4897979_4897980insACC	GRCh38
NC_000017.10:g.4801274_4801275insACC , CM000679.1:g.4801274_4801275insACC	GRCh37
NC_000017.9:g.4742053_4742054insACC	NCBI36
NG_008029.2:g.10097_10098insGTG
NG_028005.1:g.69640_69641insACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355280.11:c.*692_*693insACC (MINK1) MANE Select	ENSP00000347427.6:n.*692_*693insACC
ENST00000649488.2:c.*757_*758insGTG (CHRNE) MANE Select	ENSP00000497829.1:n.*757_*758insGTG
ENST00000652550.1:n.1965_1966insGTG (CHRNE)
ENST00000293780.4:c.*757_*758insGTG (CHRNE)	ENSP00000293780.4:n.*757_*758insGTG
ENST00000347992.11:c.*692_*693insACC (MINK1)	ENSP00000269296.7:n.*692_*693insACC
ENST00000355280.10:c.*692_*693insACC (MINK1)	ENSP00000347427.6:n.*692_*693insACC
ENST00000571207.5:c.4487_4488insACC (MINK1)
ENST00000574453.5:c.*4360_*4361insACC (MINK1)	ENSP00000461500.1:n.*4360_*4361insACC
ENST00000574871.1:n.3069_3070insACC (MINK1)
NM_000080.3:c.*757_*758insGTG (CHRNE)	NP_000071.1:n.*757_*758insGTG
NM_001024937.3:c.*692_*693insACC (MINK1)	NP_001020108.1:n.*692_*693insACC
NM_015716.4:c.*692_*693insACC (MINK1)	NP_056531.1:n.*692_*693insACC
NM_153827.4:c.*692_*693insACC (MINK1)	NP_722549.2:n.*692_*693insACC
NM_170663.4:c.*692_*693insACC (MINK1)	NP_733763.1:n.*692_*693insACC
XM_005256664.2:c.*692_*693insACC (MINK1)	XP_005256721.1:n.*692_*693insACC
XM_005256665.2:c.*692_*693insACC (MINK1)	XP_005256722.1:n.*692_*693insACC
XM_006721530.2:c.*692_*693insACC (MINK1)	XP_006721593.1:n.*692_*693insACC
XM_006721531.2:c.*692_*693insACC (MINK1)	XP_006721594.1:n.*692_*693insACC
XM_006721532.2:c.*692_*693insACC (MINK1)	XP_006721595.1:n.*692_*693insACC
XM_006721533.2:c.*692_*693insACC (MINK1)	XP_006721596.1:n.*692_*693insACC
XM_006721534.2:c.*692_*693insACC (MINK1)	XP_006721597.1:n.*692_*693insACC
XM_006721535.2:c.*692_*693insACC (MINK1)	XP_006721598.1:n.*692_*693insACC
XM_006721536.2:c.*692_*693insACC (MINK1)	XP_006721599.1:n.*692_*693insACC
XM_006721538.2:c.*692_*693insACC (MINK1)	XP_006721601.1:n.*692_*693insACC
XM_011523905.1:c.*692_*693insACC (MINK1)	XP_011522207.1:n.*692_*693insACC
XM_011523906.1:c.*692_*693insACC (MINK1)	XP_011522208.1:n.*692_*693insACC
XM_011523907.1:c.*692_*693insACC (MINK1)	XP_011522209.1:n.*692_*693insACC
XM_011523908.1:c.*692_*693insACC (MINK1)	XP_011522210.1:n.*692_*693insACC
NM_000080.4:c.*757_*758insGTG (CHRNE) MANE Select	NP_000071.1:n.*757_*758insGTG
NM_001321236.1:c.*692_*693insACC (MINK1)	NP_001308165.1:n.*692_*693insACC
XM_017024704.1:c.*692_*693insACC (MINK1)	XP_016880193.1:n.*692_*693insACC
XM_017024705.1:c.*692_*693insACC (MINK1)	XP_016880194.1:n.*692_*693insACC
XM_017024706.1:c.*692_*693insACC (MINK1)	XP_016880195.1:n.*692_*693insACC
XM_017024707.2:c.*692_*693insACC (MINK1)	XP_016880196.1:n.*692_*693insACC
XM_017024708.1:c.*692_*693insACC (MINK1)	XP_016880197.1:n.*692_*693insACC
XR_001752522.2:n.5036_5037insACC (MINK1)
NM_153827.5:c.*692_*693insACC (MINK1) MANE Select	NP_722549.2:n.*692_*693insACC
NM_001024937.4:c.*692_*693insACC (MINK1)	NP_001020108.1:n.*692_*693insACC
NM_001321236.2:c.*692_*693insACC (MINK1)	NP_001308165.1:n.*692_*693insACC
NM_015716.5:c.*692_*693insACC (MINK1)	NP_056531.1:n.*692_*693insACC
NM_170663.5:c.*692_*693insACC (MINK1)	NP_733763.1:n.*692_*693insACC