Canonical Allele Identifier: CA1084818807

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177404131_177404132insCA , CM000667.2:g.177404131_177404132insCA GRCh38
NC_000005.9:g.176831132_176831133insCA , CM000667.1:g.176831132_176831133insCA GRCh37
NC_000005.8:g.176763738_176763739insCA NCBI36
NG_007568.1:g.10445_10446insTG , LRG_145:g.10445_10446insTG

Transcript Alleles

HGVS Amino-acid change
ENST00000696192.1:c.*685-42_*685-41insTG (F12) ENSP00000512476.1:n.*685-42_*685-41insTG
ENST00000696193.1:c.*1389-25_*1389-24insTG (F12) ENSP00000512477.1:n.*1389-25_*1389-24insT...
ENST00000696194.1:c.*609-42_*609-41insTG (F12) ENSP00000512478.1:n.*609-42_*609-41insTG
ENST00000696195.1:n.3822-42_3822-41insTG (F12)
ENST00000696200.1:n.1122-42_1122-41insTG (F12)
ENST00000696201.1:c.1019-42_1019-41insTG (F12) ENSP00000512482.1:n.1019-42_1019-41insTG
ENST00000253496.4:c.1019-42_1019-41insTG (F12) MANE Select ENSP00000253496.3:n.1019-42_1019-41insTG
ENST00000253496.3:c.1019-42_1019-41insTG (F12) ENSP00000253496.3:n.1019-42_1019-41insTG
ENST00000502598.5:c.-45+605_-45+606insCA (GRK6) ENSP00000422873.1:n.-45+605_-45+606insCA
ENST00000502854.5:n.278-42_278-41insTG (F12)
ENST00000503736.1:n.391-42_391-41insTG (F12)
ENST00000510358.5:n.341_342insTG (F12)
NM_000505.3:c.1019-42_1019-41insTG , LRG_145t1:c.1019-42_1019-41insTG (F12) NP_000496.2:n.1019-42_1019-41insTG
XM_011534461.1:c.1019-42_1019-41insTG (F12) XP_011532763.1:n.1019-42_1019-41insTG
XM_011534462.1:c.683-42_683-41insTG (F12) XP_011532764.1:n.683-42_683-41insTG
XM_011534462.2:c.683-42_683-41insTG (F12) XP_011532764.1:n.683-42_683-41insTG
XM_017009773.2:c.1416+7057_1416+7058insCA (SLC34A1) XP_016865262.1:n.1416+7057_1416+7058insCA...
NM_000505.4:c.1019-42_1019-41insTG (F12) MANE Select NP_000496.2:n.1019-42_1019-41insTG