Canonical Allele Identifier: CA2618964770
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52809361-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52809361G>A , CM000674.2:g.52809361G>A GRCh38
NC_000012.11:g.53203145G>A , CM000674.1:g.53203145G>A GRCh37
NC_000012.10:g.51489412G>A NCBI36
NG_007380.1:g.10191C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.834+22C>T MANE Select ENSP00000448220.1:n.834+22C>T
ENST00000548097.5:c.*346+22C>T ENSP00000449755.1:n.*346+22C>T
ENST00000549295.1:n.290C>T
ENST00000551956.1:c.834+22C>T ENSP00000448220.1:n.834+22C>T
NM_002272.3:c.834+22C>T NP_002263.3:n.834+22C>T
NM_002272.4:c.834+22C>T MANE Select NP_002263.3:n.834+22C>T
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