Canonical Allele Identifier: CA772621859

Gene: MINK1 CHRNE

Linked Data

• dbSNP Id: rs767446594
• gnomAD v3: 17-4897981-C-CCTT
• gnomAD v4: 17-4897981-C-CCTT
• MyVariant Identifiers: chr17:g.4801276_4801277insCTT (hg19) ; chr17:g.4897981_4897982insCTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4897982_4897983insTTC , CM000679.2:g.4897982_4897983insTTC	GRCh38
NC_000017.10:g.4801277_4801278insTTC , CM000679.1:g.4801277_4801278insTTC	GRCh37
NC_000017.9:g.4742056_4742057insTTC	NCBI36
NG_008029.2:g.10094_10095insAAG
NG_028005.1:g.69643_69644insTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355280.11:c.*695_*696insTTC (MINK1) MANE Select	ENSP00000347427.6:n.*695_*696insTTC
ENST00000649488.2:c.*754_*755insAAG (CHRNE) MANE Select	ENSP00000497829.1:n.*754_*755insAAG
ENST00000652550.1:n.1962_1963insAAG (CHRNE)
ENST00000293780.4:c.*754_*755insAAG (CHRNE)	ENSP00000293780.4:n.*754_*755insAAG
ENST00000347992.11:c.*695_*696insTTC (MINK1)	ENSP00000269296.7:n.*695_*696insTTC
ENST00000355280.10:c.*695_*696insTTC (MINK1)	ENSP00000347427.6:n.*695_*696insTTC
ENST00000571207.5:c.4490_4491insTTC (MINK1)
ENST00000574453.5:c.*4363_*4364insTTC (MINK1)	ENSP00000461500.1:n.*4363_*4364insTTC
ENST00000574871.1:n.3072_3073insTTC (MINK1)
NM_000080.3:c.*754_*755insAAG (CHRNE)	NP_000071.1:n.*754_*755insAAG
NM_001024937.3:c.*695_*696insTTC (MINK1)	NP_001020108.1:n.*695_*696insTTC
NM_015716.4:c.*695_*696insTTC (MINK1)	NP_056531.1:n.*695_*696insTTC
NM_153827.4:c.*695_*696insTTC (MINK1)	NP_722549.2:n.*695_*696insTTC
NM_170663.4:c.*695_*696insTTC (MINK1)	NP_733763.1:n.*695_*696insTTC
XM_005256664.2:c.*695_*696insTTC (MINK1)	XP_005256721.1:n.*695_*696insTTC
XM_005256665.2:c.*695_*696insTTC (MINK1)	XP_005256722.1:n.*695_*696insTTC
XM_006721530.2:c.*695_*696insTTC (MINK1)	XP_006721593.1:n.*695_*696insTTC
XM_006721531.2:c.*695_*696insTTC (MINK1)	XP_006721594.1:n.*695_*696insTTC
XM_006721532.2:c.*695_*696insTTC (MINK1)	XP_006721595.1:n.*695_*696insTTC
XM_006721533.2:c.*695_*696insTTC (MINK1)	XP_006721596.1:n.*695_*696insTTC
XM_006721534.2:c.*695_*696insTTC (MINK1)	XP_006721597.1:n.*695_*696insTTC
XM_006721535.2:c.*695_*696insTTC (MINK1)	XP_006721598.1:n.*695_*696insTTC
XM_006721536.2:c.*695_*696insTTC (MINK1)	XP_006721599.1:n.*695_*696insTTC
XM_006721538.2:c.*695_*696insTTC (MINK1)	XP_006721601.1:n.*695_*696insTTC
XM_011523905.1:c.*695_*696insTTC (MINK1)	XP_011522207.1:n.*695_*696insTTC
XM_011523906.1:c.*695_*696insTTC (MINK1)	XP_011522208.1:n.*695_*696insTTC
XM_011523907.1:c.*695_*696insTTC (MINK1)	XP_011522209.1:n.*695_*696insTTC
XM_011523908.1:c.*695_*696insTTC (MINK1)	XP_011522210.1:n.*695_*696insTTC
NM_000080.4:c.*754_*755insAAG (CHRNE) MANE Select	NP_000071.1:n.*754_*755insAAG
NM_001321236.1:c.*695_*696insTTC (MINK1)	NP_001308165.1:n.*695_*696insTTC
XM_017024704.1:c.*695_*696insTTC (MINK1)	XP_016880193.1:n.*695_*696insTTC
XM_017024705.1:c.*695_*696insTTC (MINK1)	XP_016880194.1:n.*695_*696insTTC
XM_017024706.1:c.*695_*696insTTC (MINK1)	XP_016880195.1:n.*695_*696insTTC
XM_017024707.2:c.*695_*696insTTC (MINK1)	XP_016880196.1:n.*695_*696insTTC
XM_017024708.1:c.*695_*696insTTC (MINK1)	XP_016880197.1:n.*695_*696insTTC
XR_001752522.2:n.5039_5040insTTC (MINK1)
NM_153827.5:c.*695_*696insTTC (MINK1) MANE Select	NP_722549.2:n.*695_*696insTTC
NM_001024937.4:c.*695_*696insTTC (MINK1)	NP_001020108.1:n.*695_*696insTTC
NM_001321236.2:c.*695_*696insTTC (MINK1)	NP_001308165.1:n.*695_*696insTTC
NM_015716.5:c.*695_*696insTTC (MINK1)	NP_056531.1:n.*695_*696insTTC
NM_170663.5:c.*695_*696insTTC (MINK1)	NP_733763.1:n.*695_*696insTTC