Canonical Allele Identifier: CA626016689
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1237000726
gnomAD v2: 17-39768992-G-A
gnomAD v4: 17-41612740-G-A
MyVariant Identifiers: chr17:g.39768992G>A (hg19) chr17:g.41612740G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612740G>A , CM000679.2:g.41612740G>A GRCh38
NC_000017.10:g.39768992G>A , CM000679.1:g.39768992G>A GRCh37
NC_000017.9:g.37022518G>A NCBI36
NG_008301.1:g.5088C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-52C>T MANE Select ENSP00000301653.3:n.-52C>T
ENST00000301653.8:c.-52C>T ENSP00000301653.3:n.-52C>T
ENST00000588319.1:n.26C>T
ENST00000590990.1:c.-36-16C>T ENSP00000467105.1:n.-36-16C>T
ENST00000593067.1:c.-313+50C>T ENSP00000467124.1:n.-313+50C>T
NM_005557.3:c.-52C>T NP_005548.2:n.-52C>T
NM_005557.4:c.-52C>T MANE Select NP_005548.2:n.-52C>T
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