Canonical Allele Identifier: CA1931597177
Gene: CPN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100045488_100045489delinsGA , CM000672.2:g.100045488_100045489delinsGA GRCh38
NC_000010.10:g.101805245_101805246delinsGA , CM000672.1:g.101805245_101805246delinsGA GRCh37
NC_000010.9:g.101795235_101795236delinsGA NCBI36
NG_012060.1:g.41397_41398delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000370418.8:c.1231-2916_1231-2915delinsTC MANE Select ENSP00000359446.3:n.1231-2916_1231-2915delinsTC
ENST00000370418.7:c.1231-2916_1231-2915delinsTC ENSP00000359446.3:n.1231-2916_1231-2915delinsTC
NM_001308.2:c.1231-2916_1231-2915delinsTC NP_001299.1:n.1231-2916_1231-2915delinsTC
XM_011539299.1:c.1273-2916_1273-2915delinsTC XP_011537601.1:n.1273-2916_1273-2915delinsTC
NM_001308.3:c.1231-2916_1231-2915delinsTC MANE Select NP_001299.1:n.1231-2916_1231-2915delinsTC