Canonical Allele Identifier: CA2637841058
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624571-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624571T>G , CM000679.2:g.41624571T>G GRCh38
NC_000017.10:g.39780823T>G , CM000679.1:g.39780823T>G GRCh37
NC_000017.9:g.37034349T>G NCBI36
NG_008625.1:g.5060A>C
NG_009090.2:g.167142A>C , LRG_401:g.167142A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-62A>C MANE Select ENSP00000308452.8:n.-62A>C
ENST00000311208.12:c.-62A>C ENSP00000308452.8:n.-62A>C
ENST00000463128.5:c.-313+172A>C ENSP00000468672.1:n.-313+172A>C
ENST00000491673.1:n.5A>C
NM_000422.2:c.-62A>C NP_000413.1:n.-62A>C
NM_000422.3:c.-62A>C MANE Select NP_000413.1:n.-62A>C
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