Canonical Allele Identifier: CA2207623372
Community Standard Title: NC_000016.10:g.11435037C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11435037C= , CM000678.2:g.11435037C= GRCh38
NC_000016.9:g.11528893C= , CM000678.1:g.11528893C= GRCh37
NC_000016.8:g.11436394C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001370704.1:c.5405+625G= NP_001357633.1:n.5405+625G=
NM_001395505.1:c.5405+625G= NP_001382434.1:n.5405+625G=
ENST00000598234.5:c.5300+625G= ENSP00000470478.2:n.5300+625G=
ENST00000598234.6:c.5405+625G= ENSP00000470478.3:n.5405+625G=
ENST00000696174.1:c.5405+625G= ENSP00000512464.1:n.5405+625G=
XM_006720997.2:c.5300+625G= XP_006721060.2:n.5300+625G=
XM_017023929.1:c.5300+625G= XP_016879418.1:n.5300+625G=
XM_017023930.1:c.5207+625G= XP_016879419.1:n.5207+625G=
XM_017023931.1:c.5300+625G= XP_016879420.1:n.5300+625G=
XM_017023932.1:c.5300+625G= XP_016879421.1:n.5300+625G=
XM_017023933.1:c.5300+625G= XP_016879422.1:n.5300+625G=
XM_017023934.1:c.5300+625G= XP_016879423.1:n.5300+625G=
XM_017023935.1:c.5300+625G= XP_016879424.1:n.5300+625G=
XM_017023936.1:c.4949+625G= XP_016879425.1:n.4949+625G=
XM_017023937.1:c.5300+625G= XP_016879426.1:n.5300+625G=
XM_017023938.1:c.5300+625G= XP_016879427.1:n.5300+625G=
XM_017023939.1:c.5300+625G= XP_016879428.1:n.5300+625G=
XM_017023940.1:c.4205+625G= XP_016879429.1:n.4205+625G=
XM_017023941.1:c.3410+625G= XP_016879430.1:n.3410+625G=
XM_017023942.1:c.5300+625G= XP_016879431.1:n.5300+625G=
XM_017023943.1:c.2375+625G= XP_016879432.1:n.2375+625G=
XM_017023944.1:c.5300+625G= XP_016879433.1:n.5300+625G=
XM_017023945.1:c.5300+625G= XP_016879434.1:n.5300+625G=
XM_017023946.1:c.2189+625G= XP_016879435.1:n.2189+625G=
XM_017023947.2:c.1331+625G= XP_016879436.1:n.1331+625G=
XM_017023948.1:c.5244+625G= XP_016879437.1:n.5244+625G=
XM_017023949.1:c.5083-3808G= XP_016879438.1:n.5083-3808G=
XR_001752082.1:n.5690+625G=
XR_001752083.1:n.5690+625G=