Canonical Allele Identifier: CA360404357

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90024676G>C (hg19) ; chr5:g.90728859G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728859G>C , CM000667.2:g.90728859G>C	GRCh38
NC_000005.9:g.90024676G>C , CM000667.1:g.90024676G>C	GRCh37
NC_000005.8:g.90060432G>C	NCBI36
NG_007083.1:g.175060G>C
NG_007083.2:g.204516G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10352G>C MANE Select	ENSP00000384582.2:p.Ser3451Thr
ENST00000639431.1:c.265+52650G>C	ENSP00000491057.1:n.265+52650G>C
ENST00000640374.1:n.3496G>C
ENST00000640464.1:n.771G>C
ENST00000405460.6:c.10352G>C	ENSP00000384582.2:p.Ser3451Thr
ENST00000509621.1:c.3049G>C
NM_032119.3:c.10352G>C	NP_115495.3:p.Ser3451Thr
NR_003149.1:n.10365G>C
XM_011543675.1:c.10349G>C	XP_011541977.1:p.Ser3450Thr
XM_011543676.1:c.10271G>C	XP_011541978.1:p.Ser3424Thr
XM_011543677.1:c.7655G>C	XP_011541979.1:p.Ser2552Thr
XM_011543678.1:c.10352G>C	XP_011541980.1:p.Ser3451Thr
XM_011543679.1:c.10352G>C	XP_011541981.1:p.Ser3451Thr
XR_948560.1:n.271+12048C>G
NM_032119.4:c.10352G>C MANE Select	NP_115495.3:p.Ser3451Thr
XM_017009963.2:c.10373G>C	XP_016865452.1:p.Ser3458Thr
XM_017009964.2:c.10370G>C	XP_016865453.1:p.Ser3457Thr
XM_017009965.1:c.10370G>C	XP_016865454.1:p.Ser3457Thr
XM_017009966.2:c.10292G>C	XP_016865455.1:p.Ser3431Thr
XM_017009967.1:c.10277G>C	XP_016865456.1:p.Ser3426Thr
XM_017009968.2:c.10373G>C	XP_016865457.1:p.Ser3458Thr
XM_017009969.2:c.10373G>C	XP_016865458.1:p.Ser3458Thr
XM_017009970.2:c.10373G>C	XP_016865459.1:p.Ser3458Thr
XM_017009971.2:c.10373G>C	XP_016865460.1:p.Ser3458Thr
XM_017009972.1:c.3491G>C	XP_016865461.1:p.Ser1164Thr
XM_017009973.1:c.3470G>C	XP_016865462.1:p.Ser1157Thr
XM_017009974.2:c.10373G>C	XP_016865463.1:p.Ser3458Thr
XR_001742802.1:n.2522+12048C>G
NR_003149.2:n.10368G>C