Canonical Allele Identifier: CA643486

Gene: ARHGEF10L

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17648584C>T , CM000663.2:g.17648584C>T	GRCh38
NC_000001.10:g.17975079C>T , CM000663.1:g.17975079C>T	GRCh37
NC_000001.9:g.17847666C>T	NCBI36
NG_050860.1:g.133388C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018125.4:c.2303C>T MANE Select	NP_060595.3:p.Pro768Leu
ENST00000361221.8:c.2303C>T MANE Select	ENSP00000355060.3:p.Pro768Leu
NM_001011722.2:c.2186C>T	NP_001011722.2:p.Pro729Leu
NM_001319837.1:c.2171C>T	NP_001306766.1:p.Pro724Leu
NM_001319838.1:c.1412C>T	NP_001306767.1:p.Pro471Leu
NM_001328124.1:c.1637C>T	NP_001315053.1:p.Pro546Leu
NM_018125.3:c.2303C>T	NP_060595.3:p.Pro768Leu
NR_137287.1:n.3209C>T
NR_137287.2:n.3346C>T
NR_137288.1:n.3089C>T
NR_137288.2:n.3226C>T
ENST00000167825.5:c.920C>T	ENSP00000167825.5:p.Pro307Leu
ENST00000361221.7:c.2303C>T	ENSP00000355060.3:p.Pro768Leu
ENST00000375408.7:c.1622C>T	ENSP00000364557.3:p.Pro541Leu
ENST00000375415.5:c.2186C>T	ENSP00000364564.1:p.Pro729Leu
ENST00000466782.1:n.361C>T
ENST00000469726.5:n.2568C>T
XM_005245923.2:c.2198C>T	XP_005245980.2:p.Pro733Leu
XM_005245925.2:c.2186C>T	XP_005245982.2:p.Pro729Leu
XM_005245927.2:c.1637C>T	XP_005245984.2:p.Pro546Leu
XM_005245929.2:c.1622C>T	XP_005245986.2:p.Pro541Leu
XM_005245929.3:c.1622C>T	XP_005245986.2:p.Pro541Leu
XM_006710728.1:c.2198C>T	XP_006710791.1:p.Pro733Leu
XM_006710729.1:c.2195C>T	XP_006710792.1:p.Pro732Leu
XM_006710731.1:c.2195C>T	XP_006710794.1:p.Pro732Leu
XM_011541691.1:c.2189C>T	XP_011539993.1:p.Pro730Leu
XM_011541691.2:c.2189C>T	XP_011539993.1:p.Pro730Leu
XM_011541692.1:c.2183C>T	XP_011539994.1:p.Pro728Leu
XM_011541692.2:c.2183C>T	XP_011539994.1:p.Pro728Leu
XM_011541693.1:c.2174C>T	XP_011539995.1:p.Pro725Leu
XM_011541693.2:c.2174C>T	XP_011539995.1:p.Pro725Leu
XM_011541694.1:c.2171C>T	XP_011539996.1:p.Pro724Leu
XM_017001617.1:c.2171C>T	XP_016857106.1:p.Pro724Leu
XM_017001618.1:c.1592C>T	XP_016857107.1:p.Pro531Leu
XM_017001619.1:c.2198C>T	XP_016857108.1:p.Pro733Leu
XM_017001620.1:c.2183C>T	XP_016857109.1:p.Pro728Leu
XM_017001621.1:c.2303C>T	XP_016857110.1:p.Pro768Leu
XM_017001622.1:c.2288C>T	XP_016857111.1:p.Pro763Leu
XM_024448059.1:c.2198C>T	XP_024303827.1:p.Pro733Leu
XM_024448061.1:c.2198C>T	XP_024303829.1:p.Pro733Leu
XM_024448062.1:c.2198C>T	XP_024303830.1:p.Pro733Leu
XR_001737276.1:n.2328C>T
XR_001737277.1:n.2297-6052C>T
XR_002956988.1:n.3041-6052C>T
XR_002956989.1:n.3026-6052C>T
XR_946686.1:n.2241C>T
XR_946686.3:n.2327C>T
XR_946687.1:n.2211-6052C>T
XR_946688.1:n.2391C>T
XR_946688.2:n.2477C>T
XR_946689.1:n.2382C>T
XR_946689.2:n.2468C>T
XR_946690.1:n.2379C>T
XR_946690.2:n.2478C>T