Canonical Allele Identifier: CA360417613

Gene: RASA1

Linked Data

• COSMIC: COSM1071001
• MyVariant Identifiers: chr5:g.86564866T>C (hg19) ; chr5:g.87269049T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87269049T>C , CM000667.2:g.87269049T>C	GRCh38
NC_000005.9:g.86564866T>C , CM000667.1:g.86564866T>C	GRCh37
NC_000005.8:g.86600622T>C	NCBI36
NG_011650.1:g.5716T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000274376.11:c.539+59T>C MANE Select	ENSP00000274376.6:n.539+59T>C
ENST00000274376.10:c.539+59T>C	ENSP00000274376.6:n.539+59T>C
ENST00000456692.6:c.2T>C	ENSP00000411221.2:p.Met1Thr
ENST00000506290.1:c.-12T>C	ENSP00000420905.1:n.-12T>C
ENST00000512763.5:c.-96T>C	ENSP00000422008.1:n.-96T>C
ENST00000515800.6:c.539+59T>C	ENSP00000423395.2:n.539+59T>C
NM_002890.2:c.539+59T>C	NP_002881.1:n.539+59T>C
NM_022650.2:c.2T>C	NP_072179.1:p.Met1Thr
XM_011543525.1:c.539+59T>C	XP_011541827.1:n.539+59T>C
XM_011543526.1:c.539+59T>C	XP_011541828.1:n.539+59T>C
XM_011543527.1:c.539+59T>C	XP_011541829.1:n.539+59T>C
XM_011543525.2:c.539+59T>C	XP_011541827.1:n.539+59T>C
XM_011543527.3:c.539+59T>C	XP_011541829.1:n.539+59T>C
NM_002890.3:c.539+59T>C MANE Select	NP_002881.1:n.539+59T>C
NM_022650.3:c.2T>C	NP_072179.1:p.Met1Thr