Canonical Allele Identifier: CA2618964781
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52809367-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52809367A>G , CM000674.2:g.52809367A>G GRCh38
NC_000012.11:g.53203151A>G , CM000674.1:g.53203151A>G GRCh37
NC_000012.10:g.51489418A>G NCBI36
NG_007380.1:g.10185T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.834+16T>C MANE Select ENSP00000448220.1:n.834+16T>C
ENST00000548097.5:c.*346+16T>C ENSP00000449755.1:n.*346+16T>C
ENST00000549295.1:n.284T>C
ENST00000551956.1:c.834+16T>C ENSP00000448220.1:n.834+16T>C
NM_002272.3:c.834+16T>C NP_002263.3:n.834+16T>C
NM_002272.4:c.834+16T>C MANE Select NP_002263.3:n.834+16T>C
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