Canonical Allele Identifier: CA6576443
Gene: KRT86 HGNC NCBI
KRT81 HGNC NCBI

Linked Data

dbSNP Id: rs34187924
ExAC: 12:52681408 G / A
gnomAD v2: 12-52681408-G-A
gnomAD v3: 12-52287624-G-A
gnomAD v4: 12-52287624-G-A
COSMIC: COSM4042813
MyVariant Identifiers: chr12:g.52681408G>A (hg19) chr12:g.52287624G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52287624G>A , CM000674.2:g.52287624G>A GRCh38
NC_000012.11:g.52681408G>A , CM000674.1:g.52681408G>A GRCh37
NC_000012.10:g.50967675G>A NCBI36
NG_008184.1:g.8892C>T
NG_008086.2:g.17980G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423955.7:c.-5+11678G>A (KRT86) MANE Select ENSP00000444533.1:n.-5+11678G>A
ENST00000327741.9:c.998C>T (KRT81) MANE Select ENSP00000369349.4:p.Thr333Met
ENST00000423955.6:c.-5+11678G>A (KRT86) ENSP00000444533.1:n.-5+11678G>A
ENST00000553310.6:c.-4-14289G>A (KRT86) ENSP00000452237.3:n.-4-14289G>A
ENST00000615839.1:c.998C>T (KRT81) ENSP00000483796.1:p.Thr333Met
NM_002281.3:c.998C>T (KRT81) NP_002272.2:p.Thr333Met
XM_005268866.3:c.129+11678G>A (KRT86) XP_005268923.1:n.129+11678G>A
XM_011538334.1:c.998C>T (KRT81) XP_011536636.1:p.Thr333Met
XM_011538336.1:c.-5+11678G>A (KRT86) XP_011536638.1:n.-5+11678G>A
XM_011538337.1:c.-5+11678G>A (KRT86) XP_011536639.1:n.-5+11678G>A
XM_011538338.1:c.-5+11678G>A (KRT86) XP_011536640.1:n.-5+11678G>A
NM_001320198.1:c.-5+11678G>A (KRT86) NP_001307127.1:n.-5+11678G>A
XM_005268866.4:c.129+11678G>A (KRT86) XP_005268923.1:n.129+11678G>A
XM_017019296.1:c.-103+11678G>A (KRT86) XP_016874785.1:n.-103+11678G>A
NM_001320198.2:c.-5+11678G>A (KRT86) MANE Select NP_001307127.1:n.-5+11678G>A
NM_002281.4:c.998C>T (KRT81) MANE Select NP_002272.2:p.Thr333Met
Search 100 bp 5'
Search 100 bp 3'