Canonical Allele Identifier: CA8563243
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs763845040
ExAC: 17:39768394 C / A
gnomAD v2: 17-39768394-C-A
gnomAD v4: 17-41612142-C-A
MyVariant Identifiers: chr17:g.39768394C>A (hg19) chr17:g.41612142C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612142C>A , CM000679.2:g.41612142C>A GRCh38
NC_000017.10:g.39768394C>A , CM000679.1:g.39768394C>A GRCh37
NC_000017.9:g.37021920C>A NCBI36
NG_008301.1:g.5686G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.531+16G>T MANE Select ENSP00000301653.3:n.531+16G>T
ENST00000301653.8:c.531+16G>T ENSP00000301653.3:n.531+16G>T
ENST00000588319.1:n.624G>T
ENST00000593067.1:c.-184+16G>T ENSP00000467124.1:n.-184+16G>T
NM_005557.3:c.531+16G>T NP_005548.2:n.531+16G>T
NM_005557.4:c.531+16G>T MANE Select NP_005548.2:n.531+16G>T
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