Canonical Allele Identifier: CA12798500
Gene: ASAP1 HGNC NCBI

Linked Data

dbSNP Id: rs6984045

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.130080167T>C , CM000670.2:g.130080167T>C GRCh38
NC_000008.10:g.131092413T>C , CM000670.1:g.131092413T>C GRCh37
NC_000008.9:g.131161595T>C NCBI36
NG_030354.1:g.368494A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000518721.6:c.2573-196A>G MANE Select ENSP00000429900.1:n.2573-196A>G
ENST00000357668.2:c.2552-196A>G ENSP00000350297.2:n.2552-196A>G
ENST00000518721.5:c.2573-196A>G ENSP00000429900.1:n.2573-196A>G
ENST00000519483.5:c.642-196A>G
ENST00000520189.1:n.493-196A>G
ENST00000521075.5:c.*2555-196A>G ENSP00000428463.1:n.*2555-196A>G
ENST00000524124.5:c.2034-196A>G
NM_001247996.1:c.2552-196A>G NP_001234925.1:n.2552-196A>G
NM_018482.3:c.2573-196A>G NP_060952.2:n.2573-196A>G
XM_005250925.1:c.2582-196A>G XP_005250982.1:n.2582-196A>G
XM_006716563.2:c.2582-196A>G XP_006716626.1:n.2582-196A>G
XM_006716564.1:c.2561-196A>G XP_006716627.1:n.2561-196A>G
XM_006716565.2:c.2414-196A>G XP_006716628.1:n.2414-196A>G
XM_006716566.1:c.2411-196A>G XP_006716629.1:n.2411-196A>G
XM_006716567.2:c.2405-196A>G XP_006716630.1:n.2405-196A>G
XM_011517052.1:c.2582-196A>G XP_011515354.1:n.2582-196A>G
XM_011517053.1:c.2561-196A>G XP_011515355.1:n.2561-196A>G
NM_001362924.1:c.2582-196A>G NP_001349853.1:n.2582-196A>G
NM_001362925.1:c.2411-196A>G NP_001349854.1:n.2411-196A>G
NM_001362926.1:c.2402-196A>G NP_001349855.1:n.2402-196A>G
XM_006716563.3:c.2582-196A>G XP_006716626.1:n.2582-196A>G
XM_006716565.3:c.2414-196A>G XP_006716628.1:n.2414-196A>G
XM_011517052.2:c.2582-196A>G XP_011515354.1:n.2582-196A>G
XM_017013467.2:c.2447-196A>G XP_016868956.1:n.2447-196A>G
XM_017013468.1:c.2405-196A>G XP_016868957.1:n.2405-196A>G
NM_018482.4:c.2573-196A>G MANE Select NP_060952.2:n.2573-196A>G
NM_001362925.2:c.2411-196A>G NP_001349854.1:n.2411-196A>G
NM_001362926.2:c.2402-196A>G NP_001349855.1:n.2402-196A>G
NM_001247996.2:c.2552-196A>G NP_001234925.1:n.2552-196A>G