Canonical Allele Identifier: CA2036556463
Gene: KRT74 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52571290C= , CM000674.2:g.52571290C= GRCh38
NC_000012.11:g.52965074C= , CM000674.1:g.52965074C= GRCh37
NC_000012.10:g.51251341C= NCBI36
NG_012321.1:g.7536G=

Transcript Alleles

HGVS Amino-acid change
ENST00000305620.3:c.843+69G= MANE Select ENSP00000307240.2:n.843+69G=
ENST00000305620.2:c.843+69G= ENSP00000307240.2:n.843+69G=
ENST00000549343.5:c.843+69G= ENSP00000447447.1:n.843+69G=
NM_175053.3:c.843+69G= NP_778223.2:n.843+69G=
XM_011537902.1:c.843+69G= XP_011536204.1:n.843+69G=
NM_175053.4:c.843+69G= MANE Select NP_778223.2:n.843+69G=
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