Canonical Allele Identifier: CA360397632

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012488C>T (hg19) ; chr5:g.90716671C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716671C>T , CM000667.2:g.90716671C>T	GRCh38
NC_000005.9:g.90012488C>T , CM000667.1:g.90012488C>T	GRCh37
NC_000005.8:g.90048244C>T	NCBI36
NG_007083.1:g.162872C>T
NG_007083.2:g.192328C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9389C>T MANE Select	ENSP00000384582.2:p.Ser3130Phe
ENST00000639431.1:c.265+40462C>T	ENSP00000491057.1:n.265+40462C>T
ENST00000639473.1:n.4848C>T
ENST00000640012.1:c.3196C>T
ENST00000640374.1:n.2533C>T
ENST00000640779.1:c.4118C>T
ENST00000405460.6:c.9389C>T	ENSP00000384582.2:p.Ser3130Phe
ENST00000509621.1:c.2086C>T
NM_032119.3:c.9389C>T	NP_115495.3:p.Ser3130Phe
NR_003149.1:n.9402C>T
XM_011543675.1:c.9386C>T	XP_011541977.1:p.Ser3129Phe
XM_011543676.1:c.9308C>T	XP_011541978.1:p.Ser3103Phe
XM_011543677.1:c.6692C>T	XP_011541979.1:p.Ser2231Phe
XM_011543678.1:c.9389C>T	XP_011541980.1:p.Ser3130Phe
XM_011543679.1:c.9389C>T	XP_011541981.1:p.Ser3130Phe
XR_948560.1:n.272-862G>A
NM_032119.4:c.9389C>T MANE Select	NP_115495.3:p.Ser3130Phe
XM_017009963.2:c.9410C>T	XP_016865452.1:p.Ser3137Phe
XM_017009964.2:c.9407C>T	XP_016865453.1:p.Ser3136Phe
XM_017009965.1:c.9407C>T	XP_016865454.1:p.Ser3136Phe
XM_017009966.2:c.9329C>T	XP_016865455.1:p.Ser3110Phe
XM_017009967.1:c.9314C>T	XP_016865456.1:p.Ser3105Phe
XM_017009968.2:c.9410C>T	XP_016865457.1:p.Ser3137Phe
XM_017009969.2:c.9410C>T	XP_016865458.1:p.Ser3137Phe
XM_017009970.2:c.9410C>T	XP_016865459.1:p.Ser3137Phe
XM_017009971.2:c.9410C>T	XP_016865460.1:p.Ser3137Phe
XM_017009972.1:c.2528C>T	XP_016865461.1:p.Ser843Phe
XM_017009973.1:c.2507C>T	XP_016865462.1:p.Ser836Phe
XM_017009974.2:c.9410C>T	XP_016865463.1:p.Ser3137Phe
XR_001742802.1:n.2523-862G>A
NR_003149.2:n.9405C>T