Canonical Allele Identifier: CA2260099766

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612431A= , CM000679.2:g.41612431A=	GRCh38
NC_000017.10:g.39768683A= , CM000679.1:g.39768683A=	GRCh37
NC_000017.9:g.37022209A=	NCBI36
NG_008301.1:g.5397T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.258T= MANE Select	ENSP00000301653.3:p.Tyr86=
ENST00000301653.8:c.258T=	ENSP00000301653.3:p.Tyr86=
ENST00000588319.1:n.335T=
ENST00000593067.1:c.-312-145T=	ENSP00000467124.1:n.-312-145T=
NM_005557.3:c.258T=	NP_005548.2:p.Tyr86=
NM_005557.4:c.258T= MANE Select	NP_005548.2:p.Tyr86=