Canonical Allele Identifier: CA2136065922
Gene: SOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50152793_50152799delinsCATCTCT , CM000676.2:g.50152793_50152799delinsCATCTCT GRCh38
NC_000014.8:g.50619511_50619517delinsCATCTCT , CM000676.1:g.50619511_50619517delinsCATCTCT GRCh37
NC_000014.7:g.49689261_49689267delinsCATCTCT NCBI36
NG_051073.1:g.83895_83901delinsAGAGATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.2161+271_2161+277delinsAGAGATG MANE Select ENSP00000216373.5:n.2161+271_2161+277delinsAGAGATG
ENST00000216373.9:c.2161+271_2161+277delinsAGAGATG ENSP00000216373.5:n.2161+271_2161+277delinsAGAGATG
ENST00000543680.5:c.2062+271_2062+277delinsAGAGATG ENSP00000445328.1:n.2062+271_2062+277delinsAGAGATG
NM_006939.2:c.2161+271_2161+277delinsAGAGATG NP_008870.2:n.2161+271_2161+277delinsAGAGATG
XM_005268021.1:c.1981+271_1981+277delinsAGAGATG XP_005268078.1:n.1981+271_1981+277delinsAGAGATG
XM_011537103.1:c.2122+271_2122+277delinsAGAGATG XP_011535405.1:n.2122+271_2122+277delinsAGAGATG
XM_011537104.1:c.2161+271_2161+277delinsAGAGATG XP_011535406.1:n.2161+271_2161+277delinsAGAGATG
NM_006939.3:c.2161+271_2161+277delinsAGAGATG NP_008870.2:n.2161+271_2161+277delinsAGAGATG
NM_006939.4:c.2161+271_2161+277delinsAGAGATG MANE Select NP_008870.2:n.2161+271_2161+277delinsAGAGATG