Canonical Allele Identifier: CA2260099968

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612767T= , CM000679.2:g.41612767T=	GRCh38
NC_000017.10:g.39769019T= , CM000679.1:g.39769019T=	GRCh37
NC_000017.9:g.37022545T=	NCBI36
NG_008301.1:g.5061A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.-79A= MANE Select	ENSP00000301653.3:n.-79A=
ENST00000590990.1:c.-36-43A=	ENSP00000467105.1:n.-36-43A=
ENST00000593067.1:c.-313+23A=	ENSP00000467124.1:n.-313+23A=
NM_005557.3:c.-79A=	NP_005548.2:n.-79A=
NM_005557.4:c.-79A= MANE Select	NP_005548.2:n.-79A=