Canonical Allele Identifier: CA3261179040
Community Standard Title: NM_058216.3(RAD51C):c.730_732delinsGTG (p.Ile244Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709883_58709885delinsGTG , CM000679.2:g.58709883_58709885delinsGTG GRCh38
NC_000017.10:g.56787244_56787246delinsGTG , CM000679.1:g.56787244_56787246delinsGTG GRCh37
NC_000017.9:g.54142243_54142245delinsGTG NCBI36
NG_023199.1:g.22282_22284delinsGTG , LRG_314:g.22282_22284delinsGTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.730_732delinsGTG MANE Select NP_478123.1:p.Ile244Val
ENST00000337432.9:c.730_732delinsGTG MANE Select ENSP00000336701.4:p.Ile244Val
NM_058216.2:c.730_732delinsGTG NP_478123.1:p.Ile244Val
NR_103872.1:n.634_636delinsGTG
NR_103872.2:n.605_607delinsGTG
ENST00000337432.8:c.730_732delinsGTG ENSP00000336701.4:p.Ile244Val
ENST00000413590.5:c.368_370delinsGTG
ENST00000461271.5:c.379_381delinsGTG ENSP00000464056.1:p.Ile127Val
ENST00000461271.6:c.379_381delinsGTG ENSP00000464056.2:p.Ile127Val
ENST00000475762.5:c.*1433_*1435delinsGTG ENSP00000432421.1:n.*1433_*1435delinsGTG
ENST00000482007.5:c.*158_*160delinsGTG ENSP00000433332.1:n.*158_*160delinsGTG
ENST00000487525.5:c.*303_*305delinsGTG ENSP00000431637.1:n.*303_*305delinsGTG
ENST00000578151.1:n.65_67delinsGTG
ENST00000581221.5:n.245_247delinsGTG
ENST00000583539.5:c.730_732delinsGTG ENSP00000463121.1:p.Ile244Val
ENST00000584617.5:c.452_454delinsGTG
ENST00000584804.1:c.25_27delinsGTG ENSP00000463658.1:p.Ile9Val
ENST00000697678.1:n.632_634delinsGTG
ENST00000697679.1:n.1804_1806delinsGTG
ENST00000697680.1:c.*1594_*1596delinsGTG ENSP00000513392.1:n.*1594_*1596delinsGTG
ENST00000697681.1:c.*1891_*1893delinsGTG ENSP00000513393.1:n.*1891_*1893delinsGTG
ENST00000697683.1:c.*1594_*1596delinsGTG ENSP00000513395.1:n.*1594_*1596delinsGTG
ENST00000697684.1:n.790_792delinsGTG
ENST00000697685.1:c.*1427_*1429delinsGTG ENSP00000513396.1:n.*1427_*1429delinsGTG
ENST00000697686.1:c.379_381delinsGTG ENSP00000513397.1:p.Ile127Val
ENST00000697687.1:n.609_611delinsGTG
ENST00000697688.1:n.776_778delinsGTG
ENST00000697689.1:c.*1266_*1268delinsGTG ENSP00000513398.1:n.*1266_*1268delinsGTG
ENST00000697690.1:c.730_732delinsGTG ENSP00000513399.1:p.Ile244Val
ENST00000697691.1:c.*702_*704delinsGTG ENSP00000513400.1:n.*702_*704delinsGTG
ENST00000697692.1:c.*742_*744delinsGTG ENSP00000513401.1:n.*742_*744delinsGTG
ENST00000697694.1:c.379_381delinsGTG ENSP00000513402.1:p.Ile127Val
ENST00000697695.1:n.1337_1339delinsGTG
XM_006722001.2:c.730_732delinsGTG XP_006722064.1:p.Ile244Val
XM_006722001.4:c.730_732delinsGTG XP_006722064.1:p.Ile244Val
XM_006722002.2:c.730_732delinsGTG XP_006722065.1:p.Ile244Val
XM_006722002.4:c.730_732delinsGTG XP_006722065.1:p.Ile244Val
XM_006722004.2:c.379_381delinsGTG XP_006722067.1:p.Ile127Val
XM_006722004.3:c.379_381delinsGTG XP_006722067.1:p.Ile127Val
XM_006722005.2:c.379_381delinsGTG XP_006722068.1:p.Ile127Val
XM_006722005.3:c.379_381delinsGTG XP_006722068.1:p.Ile127Val
XM_011525092.1:c.379_381delinsGTG XP_011523394.1:p.Ile127Val
XM_011525092.2:c.379_381delinsGTG XP_011523394.1:p.Ile127Val
XM_011525093.1:c.379_381delinsGTG XP_011523395.1:p.Ile127Val
XM_011525093.2:c.379_381delinsGTG XP_011523395.1:p.Ile127Val
XM_011525094.1:c.379_381delinsGTG XP_011523396.1:p.Ile127Val
XM_011525094.2:c.379_381delinsGTG XP_011523396.1:p.Ile127Val
XM_017024914.1:c.379_381delinsGTG XP_016880403.1:p.Ile127Val
XM_017024915.1:c.379_381delinsGTG XP_016880404.1:p.Ile127Val
XM_017024916.1:c.379_381delinsGTG XP_016880405.1:p.Ile127Val
XM_017024917.1:c.379_381delinsGTG XP_016880406.1:p.Ile127Val
XM_017024918.2:c.379_381delinsGTG XP_016880407.1:p.Ile127Val
XM_017024919.1:c.379_381delinsGTG XP_016880408.1:p.Ile127Val
XR_934513.1:n.948_950delinsGTG
XR_934513.3:n.1379_1381delinsGTG
XR_934514.1:n.948_950delinsGTG
XR_934514.3:n.1379_1381delinsGTG