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Canonical Allele Identifier:
CA2260085927
Community Standard Title: NM_000526.5(KRT14):c.612T= (p.Tyr204=)
Gene: KRT14
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.41584410A= , CM000679.2:g.41584410A=
GRCh38
NC_000017.10:g.39740662A= , CM000679.1:g.39740662A=
GRCh37
NC_000017.9:g.36994188A=
NCBI36
NG_008624.1:g.7486T=
Transcript Alleles
HGVS
Amino-acid Change
NM_000526.5:c.612T=
MANE Select
NP_000517.3:p.Tyr204=
ENST00000167586.7:c.612T=
MANE Select
ENSP00000167586.6:p.Tyr204=
NM_000526.4:c.612T=
NP_000517.2:p.Tyr204=
ENST00000167586.6:c.612T=
ENSP00000167586.6:p.Tyr204=
ENST00000476662.1:n.62T=
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