Canonical Allele Identifier: CA2260099822

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612531_41612535delinsGAGAC , CM000679.2:g.41612531_41612535delinsGAGAC	GRCh38
NC_000017.10:g.39768783_39768787delinsGAGAC , CM000679.1:g.39768783_39768787delinsGAGAC	GRCh37
NC_000017.9:g.37022309_37022313delinsGAGAC	NCBI36
NG_008301.1:g.5293_5297delinsGTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.154_158delinsGTCTC MANE Select	ENSP00000301653.3:p.Val52=
ENST00000301653.8:c.154_158delinsGTCTC	ENSP00000301653.3:p.Val52=
ENST00000588319.1:n.231_235delinsGTCTC
ENST00000593067.1:c.-312-249_-312-245delinsGTCTC	ENSP00000467124.1:n.-312-249_-312-245delinsGTCTC
NM_005557.3:c.154_158delinsGTCTC	NP_005548.2:p.Val52=
NM_005557.4:c.154_158delinsGTCTC MANE Select	NP_005548.2:p.Val52=