Canonical Allele Identifier: CA913723092

Gene: KRT86 KRT81

Linked Data

• gnomAD v2: 12-52699708-T-TCA
• gnomAD v3: 12-52305924-T-TCA
• gnomAD v4: 12-52305924-T-TCA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52305924_52305925insCA , CM000674.2:g.52305924_52305925insCA	GRCh38
NC_000012.11:g.52699708_52699709insCA , CM000674.1:g.52699708_52699709insCA	GRCh37
NC_000012.10:g.50985975_50985976insCA	NCBI36
NG_008086.1:g.9060_9061insCA
NG_008086.2:g.36280_36281insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.1027-136_1027-135insCA (KRT86) MANE Select	ENSP00000444533.1:n.1027-136_1027-135insCA
ENST00000293525.5:c.1027-136_1027-135insCA (KRT86)	ENSP00000293525.5:n.1027-136_1027-135insCA
ENST00000423955.6:c.1027-136_1027-135insCA (KRT86)	ENSP00000444533.1:n.1027-136_1027-135insCA
NM_002284.3:c.1027-136_1027-135insCA (KRT86)	NP_002275.1:n.1027-136_1027-135insCA
XM_005268866.3:c.1258-136_1258-135insCA (KRT86)	XP_005268923.1:n.1258-136_1258-135insCA
XM_011538334.1:c.-212+2286_-212+2287insTG (KRT81)	XP_011536636.1:n.-212+2286_-212+2287insTG
XM_011538336.1:c.1027-136_1027-135insCA (KRT86)	XP_011536638.1:n.1027-136_1027-135insCA
XM_011538337.1:c.1027-136_1027-135insCA (KRT86)	XP_011536639.1:n.1027-136_1027-135insCA
XM_011538338.1:c.1027-136_1027-135insCA (KRT86)	XP_011536640.1:n.1027-136_1027-135insCA
NM_001320198.1:c.1027-136_1027-135insCA (KRT86)	NP_001307127.1:n.1027-136_1027-135insCA
XM_005268866.4:c.1258-136_1258-135insCA (KRT86)	XP_005268923.1:n.1258-136_1258-135insCA
XM_017019296.1:c.1027-136_1027-135insCA (KRT86)	XP_016874785.1:n.1027-136_1027-135insCA
NM_001320198.2:c.1027-136_1027-135insCA (KRT86) MANE Select	NP_001307127.1:n.1027-136_1027-135insCA