Canonical Allele Identifier: CA500206507
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768866C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612614C>A , CM000679.2:g.41612614C>A GRCh38
NC_000017.10:g.39768866C>A , CM000679.1:g.39768866C>A GRCh37
NC_000017.9:g.37022392C>A NCBI36
NG_008301.1:g.5214G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.75G>T MANE Select ENSP00000301653.3:p.Gly25=
ENST00000301653.8:c.75G>T ENSP00000301653.3:p.Gly25=
ENST00000588319.1:n.152G>T
ENST00000590990.1:c.75G>T ENSP00000467105.1:p.Gly25=
ENST00000593067.1:c.-313+176G>T ENSP00000467124.1:n.-313+176G>T
NM_005557.3:c.75G>T NP_005548.2:p.Gly25=
NM_005557.4:c.75G>T MANE Select NP_005548.2:p.Gly25=
Search 100 bp 5'
Search 100 bp 3'