Canonical Allele Identifier: CA399497478
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs752729625

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612673G>T , CM000679.2:g.41612673G>T GRCh38
NC_000017.10:g.39768925G>T , CM000679.1:g.39768925G>T GRCh37
NC_000017.9:g.37022451G>T NCBI36
NG_008301.1:g.5155C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.16C>A MANE Select ENSP00000301653.3:p.Arg6Ser
ENST00000301653.8:c.16C>A ENSP00000301653.3:p.Arg6Ser
ENST00000588319.1:n.93C>A
ENST00000590990.1:c.16C>A ENSP00000467105.1:p.Arg6Ser
ENST00000593067.1:c.-313+117C>A ENSP00000467124.1:n.-313+117C>A
NM_005557.3:c.16C>A NP_005548.2:p.Arg6Ser
NM_005557.4:c.16C>A MANE Select NP_005548.2:p.Arg6Ser