Canonical Allele Identifier: CA210858497

Gene: NRG3

Linked Data

• dbSNP Id: rs10623310
• gnomAD v2: 10-83819259-T-TAGAA
• gnomAD v3: 10-82059503-T-TAGAA
• gnomAD v4: 10-82059503-T-TAGAA
• MyVariant Identifiers: chr10:g.83819259_83819260insAGAA (hg19) ; chr10:g.82059503_82059504insAGAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.82059504_82059507dup , CM000672.2:g.82059504_82059507dup	GRCh38
NC_000010.10:g.83819260_83819263dup , CM000672.1:g.83819260_83819263dup	GRCh37
NC_000010.9:g.83809240_83809243dup	NCBI36
NG_013373.1:g.189191_189194dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372141.7:c.823+183341_823+183344dup MANE Select	ENSP00000361214.2:n.823+183341_823+183344dup
ENST00000372141.6:c.823+183341_823+183344dup	ENSP00000361214.2:n.823+183341_823+183344dup
ENST00000372142.6:c.61-107223_61-107220dup	ENSP00000361215.2:n.61-107223_61-107220dup
ENST00000404547.5:c.823+183341_823+183344dup	ENSP00000384796.1:n.823+183341_823+183344dup
ENST00000404576.6:c.136-107223_136-107220dup	ENSP00000385804.2:n.136-107223_136-107220dup
ENST00000555784.5:c.135+181409_135+181412dup	ENSP00000451858.1:n.135+181409_135+181412dup
ENST00000556918.5:c.136-107223_136-107220dup	ENSP00000451376.1:n.136-107223_136-107220dup
ENST00000602794.5:c.*371+169839_*371+169842dup	ENSP00000473669.1:n.*371+169839_*371+169842dup
NM_001010848.3:c.823+183341_823+183344dup	NP_001010848.2:n.823+183341_823+183344dup
NM_001165972.1:c.823+183341_823+183344dup	NP_001159444.1:n.823+183341_823+183344dup
NM_001165973.1:c.61-107223_61-107220dup	NP_001159445.1:n.61-107223_61-107220dup
XM_005269444.3:c.823+183341_823+183344dup	XP_005269501.1:n.823+183341_823+183344dup
XM_011539172.1:c.823+183341_823+183344dup	XP_011537474.1:n.823+183341_823+183344dup
XM_011539173.1:c.823+183341_823+183344dup	XP_011537475.1:n.823+183341_823+183344dup
XM_011539174.1:c.823+183341_823+183344dup	XP_011537476.1:n.823+183341_823+183344dup
XM_011539175.1:c.823+183341_823+183344dup	XP_011537477.1:n.823+183341_823+183344dup
XM_005269444.5:c.823+183341_823+183344dup	XP_005269501.1:n.823+183341_823+183344dup
XM_011539172.3:c.823+183341_823+183344dup	XP_011537474.1:n.823+183341_823+183344dup
XM_011539173.3:c.823+183341_823+183344dup	XP_011537475.1:n.823+183341_823+183344dup
XM_011539175.3:c.823+183341_823+183344dup	XP_011537477.1:n.823+183341_823+183344dup
XM_017015573.2:c.824-173238_824-173235dup	XP_016871062.1:n.824-173238_824-173235dup
XM_017015574.2:c.824-173238_824-173235dup	XP_016871063.1:n.824-173238_824-173235dup
XM_017015575.2:c.824-173238_824-173235dup	XP_016871064.1:n.824-173238_824-173235dup
XM_017015576.2:c.824-173238_824-173235dup	XP_016871065.1:n.824-173238_824-173235dup
XM_017015577.2:c.824-173238_824-173235dup	XP_016871066.1:n.824-173238_824-173235dup
XM_017015578.2:c.824-173238_824-173235dup	XP_016871067.1:n.824-173238_824-173235dup
XM_017015579.2:c.824-173238_824-173235dup	XP_016871068.1:n.824-173238_824-173235dup
XM_017015580.2:c.824-173238_824-173235dup	XP_016871069.1:n.824-173238_824-173235dup
XM_017015581.2:c.823+183341_823+183344dup	XP_016871070.1:n.823+183341_823+183344dup
XM_017015584.2:c.824-173238_824-173235dup	XP_016871073.1:n.824-173238_824-173235dup
XR_001747009.2:n.975-173238_975-173235dup
NM_001010848.4:c.823+183341_823+183344dup MANE Select	NP_001010848.2:n.823+183341_823+183344dup
NM_001370081.1:c.823+183341_823+183344dup	NP_001357010.1:n.823+183341_823+183344dup
NM_001370082.1:c.79-107223_79-107220dup	NP_001357011.1:n.79-107223_79-107220dup
NM_001370083.1:c.823+183341_823+183344dup	NP_001357012.1:n.823+183341_823+183344dup
NM_001370084.1:c.823+183341_823+183344dup	NP_001357013.1:n.823+183341_823+183344dup
NR_163251.1:n.971-91899_971-91896dup
NR_163252.1:n.409+181409_409+181412dup
NR_163253.1:n.810+169839_810+169842dup
NM_001165973.2:c.61-107223_61-107220dup	NP_001159445.1:n.61-107223_61-107220dup