Canonical Allele Identifier: CA499998711
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768914G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612662G>A , CM000679.2:g.41612662G>A GRCh38
NC_000017.10:g.39768914G>A , CM000679.1:g.39768914G>A GRCh37
NC_000017.9:g.37022440G>A NCBI36
NG_008301.1:g.5166C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.27C>T MANE Select ENSP00000301653.3:p.Thr9=
ENST00000301653.8:c.27C>T ENSP00000301653.3:p.Thr9=
ENST00000588319.1:n.104C>T
ENST00000590990.1:c.27C>T ENSP00000467105.1:p.Thr9=
ENST00000593067.1:c.-313+128C>T ENSP00000467124.1:n.-313+128C>T
NM_005557.3:c.27C>T NP_005548.2:p.Thr9=
NM_005557.4:c.27C>T MANE Select NP_005548.2:p.Thr9=
Search 100 bp 5'
Search 100 bp 3'