Canonical Allele Identifier: CA626018623
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1453961833
gnomAD v2: 17-39780810-A-AG
gnomAD v3: 17-41624558-A-AG
gnomAD v4: 17-41624558-A-AG
MyVariant Identifiers: chr17:g.39780810_39780811insG (hg19) chr17:g.41624558_41624559insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624562dup , CM000679.2:g.41624562dup GRCh38
NC_000017.10:g.39780814dup , CM000679.1:g.39780814dup GRCh37
NC_000017.9:g.37034340dup NCBI36
NG_008625.1:g.5072dup
NG_009090.2:g.167154dup , LRG_401:g.167154dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-50dup MANE Select ENSP00000308452.8:n.-50dup
ENST00000311208.12:c.-50dup ENSP00000308452.8:n.-50dup
ENST00000463128.5:c.-313+184dup ENSP00000468672.1:n.-313+184dup
ENST00000491673.1:n.17dup
NM_000422.2:c.-50dup NP_000413.1:n.-50dup
NM_000422.3:c.-50dup MANE Select NP_000413.1:n.-50dup
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