Canonical Allele Identifier: CA2260085539
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583723G= , CM000679.2:g.41583723G= GRCh38
NC_000017.10:g.39739975G= , CM000679.1:g.39739975G= GRCh37
NC_000017.9:g.36993501G= NCBI36
NG_008624.1:g.8173C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.927+37C= MANE Select ENSP00000167586.6:n.927+37C=
ENST00000167586.6:c.927+37C= ENSP00000167586.6:n.927+37C=
ENST00000476662.1:n.377+37C=
NM_000526.4:c.927+37C= NP_000517.2:n.927+37C=
NM_000526.5:c.927+37C= MANE Select NP_000517.3:n.927+37C=
Search 100 bp 5'
Search 100 bp 3'