Canonical Allele Identifier: CA2637840940
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624528-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624528C>T , CM000679.2:g.41624528C>T GRCh38
NC_000017.10:g.39780780C>T , CM000679.1:g.39780780C>T GRCh37
NC_000017.9:g.37034306C>T NCBI36
NG_008625.1:g.5103G>A
NG_009090.2:g.167185G>A , LRG_401:g.167185G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-19G>A MANE Select ENSP00000308452.8:n.-19G>A
ENST00000311208.12:c.-19G>A ENSP00000308452.8:n.-19G>A
ENST00000463128.5:c.-313+215G>A ENSP00000468672.1:n.-313+215G>A
ENST00000491673.1:n.48G>A
ENST00000540235.5:c.-224G>A ENSP00000441751.2:n.-224G>A
NM_000422.2:c.-19G>A NP_000413.1:n.-19G>A
NM_000422.3:c.-19G>A MANE Select NP_000413.1:n.-19G>A
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