Canonical Allele Identifier: CA8563381
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs781398796
ExAC: 17:39768947 A / G
gnomAD v2: 17-39768947-A-G
gnomAD v3: 17-41612695-A-G
gnomAD v4: 17-41612695-A-G
MyVariant Identifiers: chr17:g.39768947A>G (hg19) chr17:g.41612695A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612695A>G , CM000679.2:g.41612695A>G GRCh38
NC_000017.10:g.39768947A>G , CM000679.1:g.39768947A>G GRCh37
NC_000017.9:g.37022473A>G NCBI36
NG_008301.1:g.5133T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-7T>C MANE Select ENSP00000301653.3:n.-7T>C
ENST00000301653.8:c.-7T>C ENSP00000301653.3:n.-7T>C
ENST00000588319.1:n.71T>C
ENST00000590990.1:c.-7T>C ENSP00000467105.1:n.-7T>C
ENST00000593067.1:c.-313+95T>C ENSP00000467124.1:n.-313+95T>C
NM_005557.3:c.-7T>C NP_005548.2:n.-7T>C
NM_005557.4:c.-7T>C MANE Select NP_005548.2:n.-7T>C
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