Canonical Allele Identifier: CA145026268

Gene: ARMC2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108941984C>T , CM000668.2:g.108941984C>T	GRCh38
NC_000006.11:g.109263187C>T , CM000668.1:g.109263187C>T	GRCh37
NC_000006.10:g.109369880C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392644.9:c.1596+4985C>T MANE Select	ENSP00000376417.4:n.1596+4985C>T
ENST00000368972.7:c.1101+4985C>T	ENSP00000357968.3:n.1101+4985C>T
ENST00000392644.8:c.1596+4985C>T	ENSP00000376417.4:n.1596+4985C>T
NM_001286609.1:c.1101+4985C>T	NP_001273538.1:n.1101+4985C>T
NM_032131.5:c.1596+4985C>T	NP_115507.4:n.1596+4985C>T
XM_005267154.2:c.1596+4985C>T	XP_005267211.1:n.1596+4985C>T
XM_005267155.2:c.1596+4985C>T	XP_005267212.1:n.1596+4985C>T
XM_005267157.2:c.1101+4985C>T	XP_005267214.1:n.1101+4985C>T
XM_006715573.2:c.1596+4985C>T	XP_006715636.1:n.1596+4985C>T
XM_006715574.2:c.1101+4985C>T	XP_006715637.1:n.1101+4985C>T
XM_011536166.1:c.1596+4985C>T	XP_011534468.1:n.1596+4985C>T
XM_011536167.1:c.1596+4985C>T	XP_011534469.1:n.1596+4985C>T
XM_011536168.1:c.1596+4985C>T	XP_011534470.1:n.1596+4985C>T
XM_011536169.1:c.1596+4985C>T	XP_011534471.1:n.1596+4985C>T
XM_011536170.1:c.1596+4985C>T	XP_011534472.1:n.1596+4985C>T
XM_011536171.1:c.1269+4985C>T	XP_011534473.1:n.1269+4985C>T
XM_011536172.1:c.1101+4985C>T	XP_011534474.1:n.1101+4985C>T
XM_011536173.1:c.1596+4985C>T	XP_011534475.1:n.1596+4985C>T
XM_011536174.1:c.855+4985C>T	XP_011534476.1:n.855+4985C>T
XM_011536175.1:c.1597-3540C>T	XP_011534477.1:n.1597-3540C>T
XM_011536176.1:c.1497-11049C>T	XP_011534478.1:n.1497-11049C>T
XM_005267154.4:c.1596+4985C>T	XP_005267211.1:n.1596+4985C>T
XM_005267157.3:c.1101+4985C>T	XP_005267214.1:n.1101+4985C>T
XM_011536168.3:c.1596+4985C>T	XP_011534470.1:n.1596+4985C>T
XM_011536170.2:c.1596+4985C>T	XP_011534472.1:n.1596+4985C>T
XM_011536172.2:c.1101+4985C>T	XP_011534474.1:n.1101+4985C>T
XM_011536176.2:c.1497-11049C>T	XP_011534478.1:n.1497-11049C>T
XM_017011350.1:c.855+4985C>T	XP_016866839.1:n.855+4985C>T
XM_017011351.1:c.1597-636C>T	XP_016866840.1:n.1597-636C>T
XM_024446568.1:c.1101+4985C>T	XP_024302336.1:n.1101+4985C>T
XR_001743676.1:n.1765-3651C>T
NM_032131.6:c.1596+4985C>T MANE Select	NP_115507.4:n.1596+4985C>T
NM_001286609.2:c.1101+4985C>T	NP_001273538.1:n.1101+4985C>T