Canonical Allele Identifier: CA2637838326

Gene: KRT16

Linked Data

• gnomAD v4: 17-41612611-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612616del , CM000679.2:g.41612616del	GRCh38
NC_000017.10:g.39768868del , CM000679.1:g.39768868del	GRCh37
NC_000017.9:g.37022394del	NCBI36
NG_008301.1:g.5216del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.77del MANE Select	ENSP00000301653.3:p.Gly26AlafsTer?
ENST00000301653.8:c.77del	ENSP00000301653.3:p.Gly26AlafsTer?
ENST00000588319.1:n.154del
ENST00000590990.1:c.77del	ENSP00000467105.1:p.Gly26AlafsTer?
ENST00000593067.1:c.-313+178del	ENSP00000467124.1:n.-313+178del
NM_005557.3:c.77del	NP_005548.2:p.Gly26AlafsTer?
NM_005557.4:c.77del MANE Select	NP_005548.2:p.Gly26AlafsTer?