Canonical Allele Identifier: CA2036540507
Gene: KRT5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519909_52519939delinsGGCCACCGAAGCCACCTCCAAAGCCAGCTCC , CM000674.2:g.52519909_52519939delinsGGCCACCGAAGCCACCTCCAAAGCCAGCTCC GRCh38
NC_000012.11:g.52913693_52913723delinsGGCCACCGAAGCCACCTCCAAAGCCAGCTCC , CM000674.1:g.52913693_52913723delinsGGCCACCGAAGCCACCTCCAAAGCCAGCTCC GRCh37
NC_000012.10:g.51199960_51199990delinsGGCCACCGAAGCCACCTCCAAAGCCAGCTCC NCBI36
NG_008297.1:g.5521_5551delinsGGAGCTGGCTTTGGAGGTGGCTTCGGTGGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.358_388delinsGGAGCTGGCTTTGGAGGTGGCTTCGGTGGCC MANE Select ENSP00000252242.4:p.Gly120=
ENST00000252242.8:c.358_388delinsGGAGCTGGCTTTGGAGGTGGCTTCGGTGGCC ENSP00000252242.4:p.Gly120=
ENST00000546577.1:c.358_388delinsGGAGCTGGCTTTGGAGGTGGCTTCGGTGGCC ENSP00000449651.1:p.Gly120=
ENST00000549420.1:c.44-16_58delinsGGAGCTGGCTTTGGAGGTGGCTTCGGTGGCC
ENST00000551275.1:c.253_283delinsGGAGCTGGCTTTGGAGGTGGCTTCGGTGGCC ENSP00000448041.1:p.Gly85=
ENST00000552629.5:n.456_486delinsGGAGCTGGCTTTGGAGGTGGCTTCGGTGGCC
NM_000424.3:c.358_388delinsGGAGCTGGCTTTGGAGGTGGCTTCGGTGGCC NP_000415.2:p.Gly120=
NM_000424.4:c.358_388delinsGGAGCTGGCTTTGGAGGTGGCTTCGGTGGCC MANE Select NP_000415.2:p.Gly120=
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