Canonical Allele Identifier: CA399514029
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624509-T-C
MyVariant Identifiers: chr17:g.39780761T>C (hg19) chr17:g.41624509T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624509T>C , CM000679.2:g.41624509T>C GRCh38
NC_000017.10:g.39780761T>C , CM000679.1:g.39780761T>C GRCh37
NC_000017.9:g.37034287T>C NCBI36
NG_008625.1:g.5122A>G
NG_009090.2:g.167204A>G , LRG_401:g.167204A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.1A>G MANE Select ENSP00000308452.8:p.Met1Val
ENST00000311208.12:c.1A>G ENSP00000308452.8:p.Met1Val
ENST00000463128.5:c.-313+234A>G ENSP00000468672.1:n.-313+234A>G
ENST00000491673.1:n.67A>G
ENST00000540235.5:c.-205A>G ENSP00000441751.2:n.-205A>G
NM_000422.2:c.1A>G NP_000413.1:p.Met1Val
NM_000422.3:c.1A>G MANE Select NP_000413.1:p.Met1Val
Search 100 bp 5'
Search 100 bp 3'