Canonical Allele Identifier: CA411348255

Gene: RASD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35551713C>T , CM000684.2:g.35551713C>T	GRCh38
NC_000022.10:g.35947760C>T , CM000684.1:g.35947760C>T	GRCh37
NC_000022.9:g.34277706C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014310.4:c.482C>T MANE Select	NP_055125.2:p.Ser161Leu
ENST00000216127.5:c.482C>T MANE Select	ENSP00000216127.4:p.Ser161Leu
NM_001366725.1:c.482C>T	NP_001353654.1:p.Ser161Leu
NM_001376515.1:c.482C>T	NP_001363444.1:p.Ser161Leu
NM_001376516.1:c.482C>T	NP_001363445.1:p.Ser161Leu
NM_014310.3:c.482C>T	NP_055125.2:p.Ser161Leu
ENST00000216127.4:c.482C>T	ENSP00000216127.4:p.Ser161Leu
XM_005261442.3:c.482C>T	XP_005261499.1:p.Ser161Leu
XM_011530040.1:c.482C>T	XP_011528342.1:p.Ser161Leu
XM_011530040.2:c.482C>T	XP_011528342.1:p.Ser161Leu
XM_017028701.1:c.518C>T	XP_016884190.1:p.Ser173Leu
XM_017028702.1:c.482C>T	XP_016884191.1:p.Ser161Leu