Canonical Allele Identifier: CA2036556468
Gene: KRT74 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52571296G= , CM000674.2:g.52571296G= GRCh38
NC_000012.11:g.52965080G= , CM000674.1:g.52965080G= GRCh37
NC_000012.10:g.51251347G= NCBI36
NG_012321.1:g.7530C=

Transcript Alleles

HGVS Amino-acid change
ENST00000305620.3:c.843+63C= MANE Select ENSP00000307240.2:n.843+63C=
ENST00000305620.2:c.843+63C= ENSP00000307240.2:n.843+63C=
ENST00000549343.5:c.843+63C= ENSP00000447447.1:n.843+63C=
NM_175053.3:c.843+63C= NP_778223.2:n.843+63C=
XM_011537902.1:c.843+63C= XP_011536204.1:n.843+63C=
NM_175053.4:c.843+63C= MANE Select NP_778223.2:n.843+63C=