Canonical Allele Identifier: CA360363466

Gene: RASA1 CCNH

Linked Data

• MyVariant Identifiers: chr5:g.86645031T>A (hg19) ; chr5:g.87349214T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87349214T>A , CM000667.2:g.87349214T>A	GRCh38
NC_000005.9:g.86645031T>A , CM000667.1:g.86645031T>A	GRCh37
NC_000005.8:g.86680787T>A	NCBI36
NG_011650.1:g.85881T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000274376.11:c.1103T>A (RASA1) MANE Select	ENSP00000274376.6:p.Val368Asp
ENST00000645953.1:c.*91-30317A>T (CCNH)	ENSP00000494460.1:n.*91-30317A>T
ENST00000274376.10:c.1103T>A (RASA1)	ENSP00000274376.6:p.Val368Asp
ENST00000456692.6:c.572T>A (RASA1)	ENSP00000411221.2:p.Val191Asp
ENST00000506290.1:c.605T>A (RASA1)	ENSP00000420905.1:p.Val202Asp
ENST00000509953.1:n.206T>A (RASA1)
ENST00000512763.5:c.602T>A (RASA1)	ENSP00000422008.1:p.Val201Asp
ENST00000515800.6:c.1103T>A (RASA1)	ENSP00000423395.2:p.Val368Asp
NM_002890.2:c.1103T>A (RASA1)	NP_002881.1:p.Val368Asp
NM_022650.2:c.572T>A (RASA1)	NP_072179.1:p.Val191Asp
XM_011543525.1:c.1103T>A (RASA1)	XP_011541827.1:p.Val368Asp
XM_011543526.1:c.1103T>A (RASA1)	XP_011541828.1:p.Val368Asp
XM_011543527.1:c.1103T>A (RASA1)	XP_011541829.1:p.Val368Asp
NM_001364075.1:c.934-36419A>T (CCNH)	NP_001351004.1:n.934-36419A>T
NR_157068.1:n.1448-36419A>T (CCNH)
NR_157069.1:n.1041-36419A>T (CCNH)
NR_157070.1:n.1205-36419A>T (CCNH)
XM_011543525.2:c.1103T>A (RASA1)	XP_011541827.1:p.Val368Asp
XM_011543527.3:c.1103T>A (RASA1)	XP_011541829.1:p.Val368Asp
NM_001364075.2:c.934-36419A>T (CCNH)	NP_001351004.1:n.934-36419A>T
NM_002890.3:c.1103T>A (RASA1) MANE Select	NP_002881.1:p.Val368Asp
NR_157068.2:n.1448-36419A>T (CCNH)
NR_157069.2:n.1041-36419A>T (CCNH)
NR_157070.2:n.1205-36419A>T (CCNH)
NM_022650.3:c.572T>A (RASA1)	NP_072179.1:p.Val191Asp