Canonical Allele Identifier: CA2838315475

Gene: NRG3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.82198587_82198588insG , CM000672.2:g.82198587_82198588insG	GRCh38
NC_000010.10:g.83958343_83958344insG , CM000672.1:g.83958343_83958344insG	GRCh37
NC_000010.9:g.83948323_83948324insG	NCBI36
NG_013373.1:g.328274_328275insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372141.7:c.824-160152_824-160151insG MANE Select	ENSP00000361214.2:n.824-160152_824-160151insG
ENST00000372141.6:c.824-160152_824-160151insG	ENSP00000361214.2:n.824-160152_824-160151insG
ENST00000372142.6:c.160+31761_160+31762insG	ENSP00000361215.2:n.160+31761_160+31762insG
ENST00000404547.5:c.824-160152_824-160151insG	ENSP00000384796.1:n.824-160152_824-160151insG
ENST00000404576.6:c.235+31761_235+31762insG	ENSP00000385804.2:n.235+31761_235+31762insG
ENST00000555784.5:c.136-160152_136-160151insG	ENSP00000451858.1:n.136-160152_136-160151insG
ENST00000556918.5:c.235+31761_235+31762insG	ENSP00000451376.1:n.235+31761_235+31762insG
ENST00000602794.5:c.*372-160152_*372-160151insG	ENSP00000473669.1:n.*372-160152_*372-160151insG
NM_001010848.3:c.824-160152_824-160151insG	NP_001010848.2:n.824-160152_824-160151insG
NM_001165972.1:c.824-160152_824-160151insG	NP_001159444.1:n.824-160152_824-160151insG
NM_001165973.1:c.160+31761_160+31762insG	NP_001159445.1:n.160+31761_160+31762insG
XM_005269444.3:c.824-160152_824-160151insG	XP_005269501.1:n.824-160152_824-160151insG
XM_011539172.1:c.824-160152_824-160151insG	XP_011537474.1:n.824-160152_824-160151insG
XM_011539173.1:c.824-160152_824-160151insG	XP_011537475.1:n.824-160152_824-160151insG
XM_011539174.1:c.824-160152_824-160151insG	XP_011537476.1:n.824-160152_824-160151insG
XM_011539175.1:c.824-160152_824-160151insG	XP_011537477.1:n.824-160152_824-160151insG
XM_005269444.5:c.824-160152_824-160151insG	XP_005269501.1:n.824-160152_824-160151insG
XM_011539172.3:c.824-160152_824-160151insG	XP_011537474.1:n.824-160152_824-160151insG
XM_011539173.3:c.824-160152_824-160151insG	XP_011537475.1:n.824-160152_824-160151insG
XM_011539175.3:c.824-160152_824-160151insG	XP_011537477.1:n.824-160152_824-160151insG
XM_017015573.2:c.824-34155_824-34154insG	XP_016871062.1:n.824-34155_824-34154insG
XM_017015574.2:c.824-34155_824-34154insG	XP_016871063.1:n.824-34155_824-34154insG
XM_017015575.2:c.824-34155_824-34154insG	XP_016871064.1:n.824-34155_824-34154insG
XM_017015576.2:c.824-34155_824-34154insG	XP_016871065.1:n.824-34155_824-34154insG
XM_017015577.2:c.824-34155_824-34154insG	XP_016871066.1:n.824-34155_824-34154insG
XM_017015578.2:c.824-34155_824-34154insG	XP_016871067.1:n.824-34155_824-34154insG
XM_017015579.2:c.824-34155_824-34154insG	XP_016871068.1:n.824-34155_824-34154insG
XM_017015580.2:c.824-34155_824-34154insG	XP_016871069.1:n.824-34155_824-34154insG
XM_017015581.2:c.824-160152_824-160151insG	XP_016871070.1:n.824-160152_824-160151insG
XM_017015582.1:c.-36+31761_-36+31762insG	XP_016871071.1:n.-36+31761_-36+31762insG
XM_017015583.1:c.-36+31761_-36+31762insG	XP_016871072.1:n.-36+31761_-36+31762insG
XM_017015584.2:c.824-34155_824-34154insG	XP_016871073.1:n.824-34155_824-34154insG
XR_001747009.2:n.975-34155_975-34154insG
NM_001010848.4:c.824-160152_824-160151insG MANE Select	NP_001010848.2:n.824-160152_824-160151insG
NM_001370081.1:c.824-160152_824-160151insG	NP_001357010.1:n.824-160152_824-160151insG
NM_001370082.1:c.178+31761_178+31762insG	NP_001357011.1:n.178+31761_178+31762insG
NM_001370083.1:c.824-160152_824-160151insG	NP_001357012.1:n.824-160152_824-160151insG
NM_001370084.1:c.824-160152_824-160151insG	NP_001357013.1:n.824-160152_824-160151insG
NR_163251.1:n.1174+46981_1174+46982insG
NR_163252.1:n.410-160152_410-160151insG
NR_163253.1:n.811-160152_811-160151insG
NM_001165973.2:c.160+31761_160+31762insG	NP_001159445.1:n.160+31761_160+31762insG