Canonical Allele Identifier: CA2260099965

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612761G= , CM000679.2:g.41612761G=	GRCh38
NC_000017.10:g.39769013G= , CM000679.1:g.39769013G=	GRCh37
NC_000017.9:g.37022539G=	NCBI36
NG_008301.1:g.5067C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.-73C= MANE Select	ENSP00000301653.3:n.-73C=
ENST00000588319.1:n.5C=
ENST00000590990.1:c.-36-37C=	ENSP00000467105.1:n.-36-37C=
ENST00000593067.1:c.-313+29C=	ENSP00000467124.1:n.-313+29C=
NM_005557.3:c.-73C=	NP_005548.2:n.-73C=
NM_005557.4:c.-73C= MANE Select	NP_005548.2:n.-73C=