Canonical Allele Identifier: CA1603608799

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177404083C= , CM000667.2:g.177404083C= GRCh38
NC_000005.9:g.176831084C= , CM000667.1:g.176831084C= GRCh37
NC_000005.8:g.176763690C= NCBI36
NG_007568.1:g.10494G= , LRG_145:g.10494G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696192.1:c.*692G= (F12) ENSP00000512476.1:n.*692G=
ENST00000696193.1:c.*1413G= (F12) ENSP00000512477.1:n.*1413G=
ENST00000696194.1:c.*616G= (F12) ENSP00000512478.1:n.*616G=
ENST00000696195.1:n.3829G= (F12)
ENST00000696200.1:n.1129G= (F12)
ENST00000696201.1:c.1026G= (F12) ENSP00000512482.1:p.Pro342=
ENST00000253496.4:c.1026G= (F12) MANE Select ENSP00000253496.3:p.Pro342=
ENST00000253496.3:c.1026G= (F12) ENSP00000253496.3:p.Pro342=
ENST00000502598.5:c.-45+557C= (GRK6) ENSP00000422873.1:n.-45+557C=
ENST00000502854.5:n.285G= (F12)
ENST00000503736.1:n.398G= (F12)
ENST00000510358.5:n.390G= (F12)
NM_000505.3:c.1026G= , LRG_145t1:c.1026G= (F12) NP_000496.2:p.Pro342=
XM_011534461.1:c.1026G= (F12) XP_011532763.1:p.Pro342=
XM_011534462.1:c.690G= (F12) XP_011532764.1:p.Pro230=
XM_011534462.2:c.690G= (F12) XP_011532764.1:p.Pro230=
XM_017009773.2:c.1416+7009C= (SLC34A1) XP_016865262.1:n.1416+7009C=
NM_000505.4:c.1026G= (F12) MANE Select NP_000496.2:p.Pro342=