Canonical Allele Identifier: CA399497680

Gene: KRT16

Linked Data

• dbSNP Id: rs1390303879
• MyVariant Identifiers: chr17:g.39768939A>T (hg19) ; chr17:g.41612687A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612687A>T , CM000679.2:g.41612687A>T	GRCh38
NC_000017.10:g.39768939A>T , CM000679.1:g.39768939A>T	GRCh37
NC_000017.9:g.37022465A>T	NCBI36
NG_008301.1:g.5141T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.2T>A MANE Select	ENSP00000301653.3:p.Met1Lys
ENST00000301653.8:c.2T>A	ENSP00000301653.3:p.Met1Lys
ENST00000588319.1:n.79T>A
ENST00000590990.1:c.2T>A	ENSP00000467105.1:p.Met1Lys
ENST00000593067.1:c.-313+103T>A	ENSP00000467124.1:n.-313+103T>A
NM_005557.3:c.2T>A	NP_005548.2:p.Met1Lys
NM_005557.4:c.2T>A MANE Select	NP_005548.2:p.Met1Lys