Canonical Allele Identifier: CA2695225887

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612651_41612657del , CM000679.2:g.41612651_41612657del	GRCh38
NC_000017.10:g.39768903_39768909del , CM000679.1:g.39768903_39768909del	GRCh37
NC_000017.9:g.37022429_37022435del	NCBI36
NG_008301.1:g.5172_5178del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.33_39del MANE Select	ENSP00000301653.3:p.Ser12Ter
ENST00000301653.8:c.33_39del	ENSP00000301653.3:p.Ser12Ter
ENST00000588319.1:n.110_116del
ENST00000590990.1:c.33_39del	ENSP00000467105.1:p.Ser12Ter
ENST00000593067.1:c.-313+134_-313+140del	ENSP00000467124.1:n.-313+134_-313+140del
NM_005557.3:c.33_39del	NP_005548.2:p.Ser12Ter
NM_005557.4:c.33_39del MANE Select	NP_005548.2:p.Ser12Ter