Canonical Allele Identifier: CA237190562

Gene: KRT86

Linked Data

• dbSNP Id: rs924893677
• MyVariant Identifiers: chr12:g.52679519T>A (hg19) ; chr12:g.52285735T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52285735T>A , CM000674.2:g.52285735T>A	GRCh38
NC_000012.11:g.52679519T>A , CM000674.1:g.52679519T>A	GRCh37
NC_000012.10:g.50965786T>A	NCBI36
NG_008184.1:g.10781A>T
NG_008086.2:g.16091T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+9789T>A MANE Select	ENSP00000444533.1:n.-5+9789T>A
ENST00000423955.6:c.-5+9789T>A	ENSP00000444533.1:n.-5+9789T>A
ENST00000553310.6:c.-4-16178T>A	ENSP00000452237.3:n.-4-16178T>A
XM_005268866.3:c.129+9789T>A	XP_005268923.1:n.129+9789T>A
XM_011538336.1:c.-5+9789T>A	XP_011536638.1:n.-5+9789T>A
XM_011538337.1:c.-5+9789T>A	XP_011536639.1:n.-5+9789T>A
XM_011538338.1:c.-5+9789T>A	XP_011536640.1:n.-5+9789T>A
NM_001320198.1:c.-5+9789T>A	NP_001307127.1:n.-5+9789T>A
XM_005268866.4:c.129+9789T>A	XP_005268923.1:n.129+9789T>A
XM_017019296.1:c.-103+9789T>A	XP_016874785.1:n.-103+9789T>A
NM_001320198.2:c.-5+9789T>A MANE Select	NP_001307127.1:n.-5+9789T>A