Canonical Allele Identifier: CA2036689777
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52809320A= , CM000674.2:g.52809320A= GRCh38
NC_000012.11:g.53203104A= , CM000674.1:g.53203104A= GRCh37
NC_000012.10:g.51489371A= NCBI36
NG_007380.1:g.10232T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.834+63T= MANE Select ENSP00000448220.1:n.834+63T=
ENST00000548097.5:c.*346+63T= ENSP00000449755.1:n.*346+63T=
ENST00000549295.1:n.331T=
ENST00000551956.1:c.834+63T= ENSP00000448220.1:n.834+63T=
NM_002272.3:c.834+63T= NP_002263.3:n.834+63T=
NM_002272.4:c.834+63T= MANE Select NP_002263.3:n.834+63T=