Canonical Allele Identifier: CA2260099919

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612683G= , CM000679.2:g.41612683G=	GRCh38
NC_000017.10:g.39768935G= , CM000679.1:g.39768935G=	GRCh37
NC_000017.9:g.37022461G=	NCBI36
NG_008301.1:g.5145C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.6C= MANE Select	ENSP00000301653.3:p.Thr2=
ENST00000301653.8:c.6C=	ENSP00000301653.3:p.Thr2=
ENST00000588319.1:n.83C=
ENST00000590990.1:c.6C=	ENSP00000467105.1:p.Thr2=
ENST00000593067.1:c.-313+107C=	ENSP00000467124.1:n.-313+107C=
NM_005557.3:c.6C=	NP_005548.2:p.Thr2=
NM_005557.4:c.6C= MANE Select	NP_005548.2:p.Thr2=