Canonical Allele Identifier: CA2036689805
Gene: KRT4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52809355T= , CM000674.2:g.52809355T= GRCh38
NC_000012.11:g.53203139T= , CM000674.1:g.53203139T= GRCh37
NC_000012.10:g.51489406T= NCBI36
NG_007380.1:g.10197A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.834+28A= MANE Select ENSP00000448220.1:n.834+28A=
ENST00000548097.5:c.*346+28A= ENSP00000449755.1:n.*346+28A=
ENST00000549295.1:n.296A=
ENST00000551956.1:c.834+28A= ENSP00000448220.1:n.834+28A=
NM_002272.3:c.834+28A= NP_002263.3:n.834+28A=
NM_002272.4:c.834+28A= MANE Select NP_002263.3:n.834+28A=
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