Canonical Allele Identifier: CA2618897063

Gene: KRT86

Linked Data

• gnomAD v4: 12-52285818-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52285818C>T , CM000674.2:g.52285818C>T	GRCh38
NC_000012.11:g.52679602C>T , CM000674.1:g.52679602C>T	GRCh37
NC_000012.10:g.50965869C>T	NCBI36
NG_008184.1:g.10698G>A
NG_008086.2:g.16174C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+9872C>T MANE Select	ENSP00000444533.1:n.-5+9872C>T
ENST00000423955.6:c.-5+9872C>T	ENSP00000444533.1:n.-5+9872C>T
ENST00000553310.6:c.-4-16095C>T	ENSP00000452237.3:n.-4-16095C>T
XM_005268866.3:c.129+9872C>T	XP_005268923.1:n.129+9872C>T
XM_011538336.1:c.-5+9872C>T	XP_011536638.1:n.-5+9872C>T
XM_011538337.1:c.-5+9872C>T	XP_011536639.1:n.-5+9872C>T
XM_011538338.1:c.-5+9872C>T	XP_011536640.1:n.-5+9872C>T
NM_001320198.1:c.-5+9872C>T	NP_001307127.1:n.-5+9872C>T
XM_005268866.4:c.129+9872C>T	XP_005268923.1:n.129+9872C>T
XM_017019296.1:c.-103+9872C>T	XP_016874785.1:n.-103+9872C>T
NM_001320198.2:c.-5+9872C>T MANE Select	NP_001307127.1:n.-5+9872C>T