Canonical Allele Identifier: CA13021118

Gene: RAPGEF1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131597634C>G , CM000671.2:g.131597634C>G	GRCh38
NC_000009.11:g.134473021C>G , CM000671.1:g.134473021C>G	GRCh37
NC_000009.10:g.133462842C>G	NCBI36
NG_050622.1:g.147311G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372190.8:c.2109+565G>C	ENSP00000361264.3:n.2109+565G>C
ENST00000419442.2:n.1541+565G>C
ENST00000683357.1:c.2613+565G>C MANE Select	ENSP00000508246.1:n.2613+565G>C
ENST00000372189.7:c.2055+565G>C	ENSP00000361263.2:n.2055+565G>C
ENST00000372190.7:c.2109+565G>C	ENSP00000361264.3:n.2109+565G>C
ENST00000372195.5:c.2106+565G>C	ENSP00000361269.1:n.2106+565G>C
ENST00000414781.1:c.337+565G>C
NM_001304275.1:c.2106+565G>C	NP_001291204.1:n.2106+565G>C
NM_005312.3:c.2055+565G>C	NP_005303.2:n.2055+565G>C
NM_198679.1:c.2109+565G>C	NP_941372.1:n.2109+565G>C
XM_005272186.3:c.2616+565G>C	XP_005272243.1:n.2616+565G>C
XM_005272191.2:c.2502+565G>C	XP_005272248.1:n.2502+565G>C
XM_006717067.2:c.2634+565G>C	XP_006717130.1:n.2634+565G>C
XM_006717072.2:c.2520+565G>C	XP_006717135.1:n.2520+565G>C
XM_006717074.2:c.2124+565G>C	XP_006717137.1:n.2124+565G>C
XM_011518569.1:c.2658+565G>C	XP_011516871.1:n.2658+565G>C
XM_011518570.1:c.2655+565G>C	XP_011516872.1:n.2655+565G>C
XM_011518571.1:c.2643+565G>C	XP_011516873.1:n.2643+565G>C
XM_011518572.1:c.2640+565G>C	XP_011516874.1:n.2640+565G>C
XM_011518573.1:c.2589+565G>C	XP_011516875.1:n.2589+565G>C
XM_011518574.1:c.2565+565G>C	XP_011516876.1:n.2565+565G>C
XM_011518575.1:c.2562+565G>C	XP_011516877.1:n.2562+565G>C
XM_011518576.1:c.2307+565G>C	XP_011516878.1:n.2307+565G>C
XM_011518577.1:c.2304+565G>C	XP_011516879.1:n.2304+565G>C
XM_011518578.1:c.2241+565G>C	XP_011516880.1:n.2241+565G>C
XM_011518579.1:c.2148+565G>C	XP_011516881.1:n.2148+565G>C
XR_929778.1:n.2830+565G>C
XM_005272186.4:c.2616+565G>C	XP_005272243.1:n.2616+565G>C
XM_005272191.3:c.2502+565G>C	XP_005272248.1:n.2502+565G>C
XM_006717067.3:c.2634+565G>C	XP_006717130.1:n.2634+565G>C
XM_006717072.3:c.2520+565G>C	XP_006717135.1:n.2520+565G>C
XM_006717074.3:c.2124+565G>C	XP_006717137.1:n.2124+565G>C
XM_011518569.3:c.2658+565G>C	XP_011516871.1:n.2658+565G>C
XM_011518570.3:c.2655+565G>C	XP_011516872.1:n.2655+565G>C
XM_011518571.2:c.2643+565G>C	XP_011516873.1:n.2643+565G>C
XM_011518572.2:c.2640+565G>C	XP_011516874.1:n.2640+565G>C
XM_011518573.3:c.2589+565G>C	XP_011516875.1:n.2589+565G>C
XM_011518574.3:c.2565+565G>C	XP_011516876.1:n.2565+565G>C
XM_011518575.3:c.2562+565G>C	XP_011516877.1:n.2562+565G>C
XM_011518576.3:c.2307+565G>C	XP_011516878.1:n.2307+565G>C
XM_011518577.3:c.2304+565G>C	XP_011516879.1:n.2304+565G>C
XM_011518578.3:c.2241+565G>C	XP_011516880.1:n.2241+565G>C
XM_011518579.3:c.2148+565G>C	XP_011516881.1:n.2148+565G>C
XM_017014633.1:c.2565+565G>C	XP_016870122.1:n.2565+565G>C
XM_017014634.1:c.2547+565G>C	XP_016870123.1:n.2547+565G>C
XM_017014635.2:c.2547+565G>C	XP_016870124.1:n.2547+565G>C
XM_017014636.2:c.2523+565G>C	XP_016870125.1:n.2523+565G>C
XM_017014637.2:c.2499+565G>C	XP_016870126.1:n.2499+565G>C
XM_017014638.2:c.2406+565G>C	XP_016870127.1:n.2406+565G>C
XM_017014639.2:c.2400+565G>C	XP_016870128.1:n.2400+565G>C
XM_017014640.2:c.2658+565G>C	XP_016870129.1:n.2658+565G>C
XM_017014641.2:c.2658+565G>C	XP_016870130.1:n.2658+565G>C
XM_024447521.1:c.2103+565G>C	XP_024303289.1:n.2103+565G>C
XR_001746282.2:n.2834+565G>C
NM_001304275.2:c.2106+565G>C	NP_001291204.1:n.2106+565G>C
NM_001377935.1:c.2613+565G>C MANE Select	NP_001364864.1:n.2613+565G>C
NM_001377936.1:c.2052+565G>C	NP_001364865.1:n.2052+565G>C
NM_001377937.1:c.1992+565G>C	NP_001364866.1:n.1992+565G>C
NM_001377938.1:c.2502+565G>C	NP_001364867.1:n.2502+565G>C
NM_005312.4:c.2055+565G>C	NP_005303.2:n.2055+565G>C
NM_198679.2:c.2109+565G>C	NP_941372.1:n.2109+565G>C