Canonical Allele Identifier: CA399495330
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768654C>T (hg19) chr17:g.41612402C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612402C>T , CM000679.2:g.41612402C>T GRCh38
NC_000017.10:g.39768654C>T , CM000679.1:g.39768654C>T GRCh37
NC_000017.9:g.37022180C>T NCBI36
NG_008301.1:g.5426G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.287G>A MANE Select ENSP00000301653.3:p.Gly96Asp
ENST00000301653.8:c.287G>A ENSP00000301653.3:p.Gly96Asp
ENST00000588319.1:n.364G>A
ENST00000593067.1:c.-312-116G>A ENSP00000467124.1:n.-312-116G>A
NM_005557.3:c.287G>A NP_005548.2:p.Gly96Asp
NM_005557.4:c.287G>A MANE Select NP_005548.2:p.Gly96Asp
Search 100 bp 5'
Search 100 bp 3'