Canonical Allele Identifier: CA689822465

Gene: KRT86

Linked Data

• dbSNP Id: rs1343225663
• gnomAD v3: 12-52285752-C-CT
• gnomAD v4: 12-52285752-C-CT
• MyVariant Identifiers: chr12:g.52679536_52679537insT (hg19) ; chr12:g.52285752_52285753insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52285753dup , CM000674.2:g.52285753dup	GRCh38
NC_000012.11:g.52679537dup , CM000674.1:g.52679537dup	GRCh37
NC_000012.10:g.50965804dup	NCBI36
NG_008184.1:g.10763dup
NG_008086.2:g.16109dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+9807dup MANE Select	ENSP00000444533.1:n.-5+9807dup
ENST00000423955.6:c.-5+9807dup	ENSP00000444533.1:n.-5+9807dup
ENST00000553310.6:c.-4-16160dup	ENSP00000452237.3:n.-4-16160dup
XM_005268866.3:c.129+9807dup	XP_005268923.1:n.129+9807dup
XM_011538336.1:c.-5+9807dup	XP_011536638.1:n.-5+9807dup
XM_011538337.1:c.-5+9807dup	XP_011536639.1:n.-5+9807dup
XM_011538338.1:c.-5+9807dup	XP_011536640.1:n.-5+9807dup
NM_001320198.1:c.-5+9807dup	NP_001307127.1:n.-5+9807dup
XM_005268866.4:c.129+9807dup	XP_005268923.1:n.129+9807dup
XM_017019296.1:c.-103+9807dup	XP_016874785.1:n.-103+9807dup
NM_001320198.2:c.-5+9807dup MANE Select	NP_001307127.1:n.-5+9807dup