Canonical Allele Identifier: CA772024412
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1442013718
gnomAD v3: 17-41612708-A-G
gnomAD v4: 17-41612708-A-G
MyVariant Identifiers: chr17:g.39768960A>G (hg19) chr17:g.41612708A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612708A>G , CM000679.2:g.41612708A>G GRCh38
NC_000017.10:g.39768960A>G , CM000679.1:g.39768960A>G GRCh37
NC_000017.9:g.37022486A>G NCBI36
NG_008301.1:g.5120T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-20T>C MANE Select ENSP00000301653.3:n.-20T>C
ENST00000301653.8:c.-20T>C ENSP00000301653.3:n.-20T>C
ENST00000588319.1:n.58T>C
ENST00000590990.1:c.-20T>C ENSP00000467105.1:n.-20T>C
ENST00000593067.1:c.-313+82T>C ENSP00000467124.1:n.-313+82T>C
NM_005557.3:c.-20T>C NP_005548.2:n.-20T>C
NM_005557.4:c.-20T>C MANE Select NP_005548.2:n.-20T>C
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