Canonical Allele Identifier: CA2036663536

Gene: KRT4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52813982T= , CM000674.2:g.52813982T=	GRCh38
NC_000012.11:g.53207766T= , CM000674.1:g.53207766T=	GRCh37
NC_000012.10:g.51494033T=	NCBI36
NG_007380.1:g.5570A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.2:c.77A= MANE Select	ENSP00000448220.1:p.Lys26=
ENST00000548097.5:c.77A=	ENSP00000449755.1:p.Lys26=
ENST00000551956.1:c.77A=	ENSP00000448220.1:p.Lys26=
ENST00000552668.1:c.77A=	ENSP00000447320.1:p.Lys26=
NM_002272.3:c.77A=	NP_002263.3:p.Lys26=
NM_002272.4:c.77A= MANE Select	NP_002263.3:p.Lys26=