Canonical Allele Identifier: CA12798544
Gene: ASAP1 HGNC NCBI

Linked Data

dbSNP Id: rs3057

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.130317591C>T , CM000670.2:g.130317591C>T GRCh38
NC_000008.10:g.131329837C>T , CM000670.1:g.131329837C>T GRCh37
NC_000008.9:g.131399019C>T NCBI36
NG_030354.1:g.131070G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000518721.6:c.186+40426G>A MANE Select ENSP00000429900.1:p.=
ENST00000357668.2:c.165+40426G>A ENSP00000350297.2:p.=
ENST00000518721.5:c.186+40426G>A ENSP00000429900.1:p.=
ENST00000520927.5:c.*168+40426G>A ENSP00000428629.1:p.=
ENST00000521075.5:c.*168+40426G>A ENSP00000428463.1:p.=
ENST00000521426.5:c.165+40426G>A ENSP00000430917.1:p.=
ENST00000524299.1:c.*168+40426G>A ENSP00000429614.1:p.=
NM_001247996.1:c.165+40426G>A NP_001234925.1:p.=
NM_018482.3:c.186+40426G>A NP_060952.2:p.=
XM_005250925.1:c.186+40426G>A XP_005250982.1:p.=
XM_006716563.2:c.186+40426G>A XP_006716626.1:p.=
XM_006716564.1:c.165+40426G>A XP_006716627.1:p.=
XM_006716565.2:c.-120-27453G>A XP_006716628.1:p.=
XM_006716566.1:c.186+40426G>A XP_006716629.1:p.=
XM_006716567.2:c.10-80597G>A XP_006716630.1:p.=
XM_011517052.1:c.186+40426G>A XP_011515354.1:p.=
XM_011517053.1:c.165+40426G>A XP_011515355.1:p.=
NM_001362924.1:c.186+40426G>A NP_001349853.1:p.=
NM_001362925.1:c.186+40426G>A NP_001349854.1:p.=
NM_001362926.1:c.186+40426G>A NP_001349855.1:p.=
XM_006716563.3:c.186+40426G>A XP_006716626.1:p.=
XM_006716565.3:c.-120-27453G>A XP_006716628.1:p.=
XM_011517052.2:c.186+40426G>A XP_011515354.1:p.=
XM_017013467.2:c.51+40091G>A XP_016868956.1:p.=
XM_017013468.1:c.10-80597G>A XP_016868957.1:p.=
NM_018482.4:c.186+40426G>A MANE Select NP_060952.2:p.=
NM_001362925.2:c.186+40426G>A NP_001349854.1:p.=
NM_001362926.2:c.186+40426G>A NP_001349855.1:p.=
NM_001247996.2:c.165+40426G>A NP_001234925.1:p.=