Canonical Allele Identifier: CA2637838459

Gene: KRT16

Linked Data

• gnomAD v4: 17-41612735-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612738del , CM000679.2:g.41612738del	GRCh38
NC_000017.10:g.39768990del , CM000679.1:g.39768990del	GRCh37
NC_000017.9:g.37022516del	NCBI36
NG_008301.1:g.5092del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.-48del MANE Select	ENSP00000301653.3:n.-48del
ENST00000301653.8:c.-48del	ENSP00000301653.3:n.-48del
ENST00000588319.1:n.30del
ENST00000590990.1:c.-36-12del	ENSP00000467105.1:n.-36-12del
ENST00000593067.1:c.-313+54del	ENSP00000467124.1:n.-313+54del
NM_005557.3:c.-48del	NP_005548.2:n.-48del
NM_005557.4:c.-48del MANE Select	NP_005548.2:n.-48del