Canonical Allele Identifier: CA15526228
Gene: CALN1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11766496

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.71923865G>C , CM000669.2:g.71923865G>C GRCh38
NC_000007.12:g.71026786G>C NCBI36
NC_000007.13:g.71388850G>C , CM000669.1:g.71388850G>C GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000329008.9:c.375+99792C>G ENSP00000332498.5:p.=
ENST00000395275.6:c.501+99792C>G ENSP00000378690.2:p.=
ENST00000395276.6:c.375+99792C>G ENSP00000378691.2:p.=
ENST00000431984.5:c.375+99792C>G ENSP00000410704.1:p.=
NM_001017440.2:c.375+99792C>G NP_001017440.1:p.=
NM_031468.3:c.501+99792C>G NP_113656.2:p.=
XM_011516593.1:c.375+99792C>G XP_011514895.1:p.=
XM_011516594.1:c.426+99792C>G XP_011514896.1:p.=
XM_011516595.1:c.375+99792C>G XP_011514897.1:p.=
XM_011516596.1:c.375+99792C>G XP_011514898.1:p.=
XM_011516597.1:c.375+99792C>G XP_011514899.1:p.=
XM_011516599.1:c.375+99792C>G XP_011514901.1:p.=