Canonical Allele Identifier: CA689835294

Gene: KRT86 KRT81

Linked Data

• dbSNP Id: rs1399715603
• gnomAD v3: 12-52305846-GC-G
• gnomAD v4: 12-52305846-GC-G
• MyVariant Identifiers: chr12:g.52699631del (hg19) ; chr12:g.52305847del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52305848del , CM000674.2:g.52305848del	GRCh38
NC_000012.11:g.52699632del , CM000674.1:g.52699632del	GRCh37
NC_000012.10:g.50985899del	NCBI36
NG_008086.1:g.8984del
NG_008086.2:g.36204del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.1026+60del (KRT86) MANE Select	ENSP00000444533.1:n.1026+60del
ENST00000293525.5:c.1026+60del (KRT86)	ENSP00000293525.5:n.1026+60del
ENST00000423955.6:c.1026+60del (KRT86)	ENSP00000444533.1:n.1026+60del
NM_002284.3:c.1026+60del (KRT86)	NP_002275.1:n.1026+60del
XM_005268866.3:c.1257+60del (KRT86)	XP_005268923.1:n.1257+60del
XM_011538334.1:c.-212+2364del (KRT81)	XP_011536636.1:n.-212+2364del
XM_011538336.1:c.1026+60del (KRT86)	XP_011536638.1:n.1026+60del
XM_011538337.1:c.1026+60del (KRT86)	XP_011536639.1:n.1026+60del
XM_011538338.1:c.1026+60del (KRT86)	XP_011536640.1:n.1026+60del
NM_001320198.1:c.1026+60del (KRT86)	NP_001307127.1:n.1026+60del
XM_005268866.4:c.1257+60del (KRT86)	XP_005268923.1:n.1257+60del
XM_017019296.1:c.1026+60del (KRT86)	XP_016874785.1:n.1026+60del
NM_001320198.2:c.1026+60del (KRT86) MANE Select	NP_001307127.1:n.1026+60del