Canonical Allele Identifier: CA2796010122
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52809272G>C , CM000674.2:g.52809272G>C GRCh38
NC_000012.11:g.53203056G>C , CM000674.1:g.53203056G>C GRCh37
NC_000012.10:g.51489323G>C NCBI36
NG_007380.1:g.10280C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.834+111C>G MANE Select ENSP00000448220.1:n.834+111C>G
ENST00000548097.5:c.*346+111C>G ENSP00000449755.1:n.*346+111C>G
ENST00000549295.1:n.379C>G
ENST00000551956.1:c.834+111C>G ENSP00000448220.1:n.834+111C>G
NM_002272.3:c.834+111C>G NP_002263.3:n.834+111C>G
NM_002272.4:c.834+111C>G MANE Select NP_002263.3:n.834+111C>G