Canonical Allele Identifier: CA399496456
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs111383277

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612568G>C , CM000679.2:g.41612568G>C GRCh38
NC_000017.10:g.39768820G>C , CM000679.1:g.39768820G>C GRCh37
NC_000017.9:g.37022346G>C NCBI36
NG_008301.1:g.5260C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.121C>G MANE Select ENSP00000301653.3:p.Arg41Gly
ENST00000301653.8:c.121C>G ENSP00000301653.3:p.Arg41Gly
ENST00000588319.1:n.198C>G
ENST00000590990.1:c.121C>G ENSP00000467105.1:p.Arg41Gly
ENST00000593067.1:c.-313+222C>G ENSP00000467124.1:n.-313+222C>G
NM_005557.3:c.121C>G NP_005548.2:p.Arg41Gly
NM_005557.4:c.121C>G MANE Select NP_005548.2:p.Arg41Gly