Canonical Allele Identifier: CA499998658
Gene: KRT16 HGNC NCBI

Linked Data

gnomAD v4: 17-41612650-G-A
MyVariant Identifiers: chr17:g.39768902G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612650G>A , CM000679.2:g.41612650G>A GRCh38
NC_000017.10:g.39768902G>A , CM000679.1:g.39768902G>A GRCh37
NC_000017.9:g.37022428G>A NCBI36
NG_008301.1:g.5178C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.39C>T MANE Select ENSP00000301653.3:p.Ser13=
ENST00000301653.8:c.39C>T ENSP00000301653.3:p.Ser13=
ENST00000588319.1:n.116C>T
ENST00000590990.1:c.39C>T ENSP00000467105.1:p.Ser13=
ENST00000593067.1:c.-313+140C>T ENSP00000467124.1:n.-313+140C>T
NM_005557.3:c.39C>T NP_005548.2:p.Ser13=
NM_005557.4:c.39C>T MANE Select NP_005548.2:p.Ser13=
Search 100 bp 5'
Search 100 bp 3'