Canonical Allele Identifier: CA2838359720

Gene: VSIG10

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.118079285T>A , CM000674.2:g.118079285T>A	GRCh38
NC_000012.11:g.118517090T>A , CM000674.1:g.118517090T>A	GRCh37
NC_000012.10:g.117001473T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359236.10:c.925+61A>T MANE Select	ENSP00000352172.5:n.925+61A>T
ENST00000359236.9:c.925+61A>T	ENSP00000352172.5:n.925+61A>T
NM_019086.5:c.925+61A>T	NP_061959.2:n.925+61A>T
XM_005253908.3:c.409+61A>T	XP_005253965.1:n.409+61A>T
XM_006719467.2:c.622+61A>T	XP_006719530.1:n.622+61A>T
XM_006719468.2:c.226+61A>T	XP_006719531.1:n.226+61A>T
XM_011538502.1:c.925+61A>T	XP_011536804.1:n.925+61A>T
XR_944592.1:n.1259+61A>T
XR_944593.1:n.1259+61A>T
XR_944594.1:n.1259+61A>T
XM_005253908.4:c.409+61A>T	XP_005253965.1:n.409+61A>T
XM_017019504.1:c.409+61A>T	XP_016874993.1:n.409+61A>T
XM_017019505.1:c.409+61A>T	XP_016874994.1:n.409+61A>T
XM_017019506.1:c.226+61A>T	XP_016874995.1:n.226+61A>T
XR_002957341.1:n.1259+61A>T
XR_002957342.1:n.1259+61A>T
XR_002957343.1:n.1259+61A>T
NM_019086.6:c.925+61A>T MANE Select	NP_061959.2:n.925+61A>T