Canonical Allele Identifier: CA3581264

Linked Data

dbSNP Id: rs763865751

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177404016T>A , CM000667.2:g.177404016T>A GRCh38
NC_000005.9:g.176831017T>A , CM000667.1:g.176831017T>A GRCh37
NC_000005.8:g.176763623T>A NCBI36
NG_007568.1:g.10561A>T , LRG_145:g.10561A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696192.1:c.*759A>T (F12) ENSP00000512476.1:n.*759A>T
ENST00000696193.1:c.*1480A>T (F12) ENSP00000512477.1:n.*1480A>T
ENST00000696194.1:c.*683A>T (F12) ENSP00000512478.1:n.*683A>T
ENST00000696195.1:n.3896A>T (F12)
ENST00000696200.1:n.1196A>T (F12)
ENST00000696201.1:c.1093A>T (F12) ENSP00000512482.1:p.Lys365Ter
ENST00000253496.4:c.1093A>T (F12) MANE Select ENSP00000253496.3:p.Lys365Ter
ENST00000253496.3:c.1093A>T (F12) ENSP00000253496.3:p.Lys365Ter
ENST00000502598.5:c.-45+490T>A (GRK6) ENSP00000422873.1:n.-45+490T>A
ENST00000502854.5:n.352A>T (F12)
ENST00000503736.1:n.465A>T (F12)
ENST00000510358.5:n.457A>T (F12)
NM_000505.3:c.1093A>T , LRG_145t1:c.1093A>T (F12) NP_000496.2:p.Lys365Ter
XM_011534461.1:c.1093A>T (F12) XP_011532763.1:p.Lys365Ter
XM_011534462.1:c.757A>T (F12) XP_011532764.1:p.Lys253Ter
XM_011534462.2:c.757A>T (F12) XP_011532764.1:p.Lys253Ter
XM_017009773.2:c.1416+6942T>A (SLC34A1) XP_016865262.1:n.1416+6942T>A
NM_000505.4:c.1093A>T (F12) MANE Select NP_000496.2:p.Lys365Ter