Canonical Allele Identifier: CA2260099779
Gene: KRT16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612471C= , CM000679.2:g.41612471C= GRCh38
NC_000017.10:g.39768723C= , CM000679.1:g.39768723C= GRCh37
NC_000017.9:g.37022249C= NCBI36
NG_008301.1:g.5357G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.218G= MANE Select ENSP00000301653.3:p.Ser73=
ENST00000301653.8:c.218G= ENSP00000301653.3:p.Ser73=
ENST00000588319.1:n.295G=
ENST00000593067.1:c.-312-185G= ENSP00000467124.1:n.-312-185G=
NM_005557.3:c.218G= NP_005548.2:p.Ser73=
NM_005557.4:c.218G= MANE Select NP_005548.2:p.Ser73=
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