Canonical Allele Identifier: CA290678318

Gene: KRT16

Linked Data

• dbSNP Id: rs981938633
• MyVariant Identifiers: chr17:g.39768979_39768980insA (hg19) ; chr17:g.41612727_41612728insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612730dup , CM000679.2:g.41612730dup	GRCh38
NC_000017.10:g.39768982dup , CM000679.1:g.39768982dup	GRCh37
NC_000017.9:g.37022508dup	NCBI36
NG_008301.1:g.5100dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.-40dup MANE Select	ENSP00000301653.3:n.-40dup
ENST00000301653.8:c.-40dup	ENSP00000301653.3:n.-40dup
ENST00000588319.1:n.38dup
ENST00000590990.1:c.-36-4dup	ENSP00000467105.1:n.-36-4dup
ENST00000593067.1:c.-313+62dup	ENSP00000467124.1:n.-313+62dup
NM_005557.3:c.-40dup	NP_005548.2:n.-40dup
NM_005557.4:c.-40dup MANE Select	NP_005548.2:n.-40dup