Canonical Allele Identifier: CA360417632

Gene: RASA1

Linked Data

• MyVariant Identifiers: chr5:g.86564873G>A (hg19) ; chr5:g.87269056G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87269056G>A , CM000667.2:g.87269056G>A	GRCh38
NC_000005.9:g.86564873G>A , CM000667.1:g.86564873G>A	GRCh37
NC_000005.8:g.86600629G>A	NCBI36
NG_011650.1:g.5723G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000274376.11:c.539+66G>A MANE Select	ENSP00000274376.6:n.539+66G>A
ENST00000274376.10:c.539+66G>A	ENSP00000274376.6:n.539+66G>A
ENST00000456692.6:c.8+1G>A	ENSP00000411221.2:n.8+1G>A
ENST00000506290.1:c.-6+1G>A	ENSP00000420905.1:n.-6+1G>A
ENST00000512763.5:c.-90+1G>A	ENSP00000422008.1:n.-90+1G>A
ENST00000515800.6:c.539+66G>A	ENSP00000423395.2:n.539+66G>A
NM_002890.2:c.539+66G>A	NP_002881.1:n.539+66G>A
NM_022650.2:c.8+1G>A	NP_072179.1:n.8+1G>A
XM_011543525.1:c.539+66G>A	XP_011541827.1:n.539+66G>A
XM_011543526.1:c.539+66G>A	XP_011541828.1:n.539+66G>A
XM_011543527.1:c.539+66G>A	XP_011541829.1:n.539+66G>A
XM_011543525.2:c.539+66G>A	XP_011541827.1:n.539+66G>A
XM_011543527.3:c.539+66G>A	XP_011541829.1:n.539+66G>A
NM_002890.3:c.539+66G>A MANE Select	NP_002881.1:n.539+66G>A
NM_022650.3:c.8+1G>A	NP_072179.1:n.8+1G>A