Canonical Allele Identifier: CA389649636

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50666498T>A (hg19) ; chr14:g.50199780T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199780T>A , CM000676.2:g.50199780T>A	GRCh38
NC_000014.8:g.50666498T>A , CM000676.1:g.50666498T>A	GRCh37
NC_000014.7:g.49736248T>A	NCBI36
NG_051073.1:g.36914A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.421A>T MANE Select	ENSP00000216373.5:p.Ile141Phe
ENST00000216373.9:c.421A>T	ENSP00000216373.5:p.Ile141Phe
ENST00000543680.5:c.421A>T	ENSP00000445328.1:p.Ile141Phe
ENST00000555666.1:n.600A>T
ENST00000556469.5:n.392A>T
NM_006939.2:c.421A>T	NP_008870.2:p.Ile141Phe
XM_005268021.1:c.241A>T	XP_005268078.1:p.Ile81Phe
XM_011537103.1:c.382A>T	XP_011535405.1:p.Ile128Phe
XM_011537104.1:c.421A>T	XP_011535406.1:p.Ile141Phe
XR_943842.1:n.1039+15908T>A
XR_943843.1:n.1039+15908T>A
NM_006939.3:c.421A>T	NP_008870.2:p.Ile141Phe
NM_006939.4:c.421A>T MANE Select	NP_008870.2:p.Ile141Phe