Canonical Allele Identifier: CA360401684

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90087020G>T (hg19) ; chr5:g.90791203G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791203G>T , CM000667.2:g.90791203G>T	GRCh38
NC_000005.9:g.90087020G>T , CM000667.1:g.90087020G>T	GRCh37
NC_000005.8:g.90122776G>T	NCBI36
NG_007083.1:g.237404G>T
NG_007083.2:g.266860G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14374G>T MANE Select	ENSP00000384582.2:p.Gly4792Ter
ENST00000425867.3:c.3328G>T	ENSP00000392618.3:p.Gly1110Ter
ENST00000507314.2:c.49G>T	ENSP00000491299.1:p.Gly17Ter
ENST00000638510.1:n.1641G>T
ENST00000638585.1:n.140G>T
ENST00000638975.1:c.1003G>T	ENSP00000492630.1:p.Gly335Ter
ENST00000639431.1:c.265+114994G>T	ENSP00000491057.1:n.265+114994G>T
ENST00000640407.1:c.784G>T	ENSP00000491425.1:p.Gly262Ter
ENST00000405460.6:c.14374G>T	ENSP00000384582.2:p.Gly4792Ter
ENST00000425867.2:c.1357G>T	ENSP00000392618.2:p.Gly453Ter
ENST00000507314.1:n.49G>T
NM_032119.3:c.14374G>T	NP_115495.3:p.Gly4792Ter
NR_003149.1:n.14387G>T
XM_011543675.1:c.14371G>T	XP_011541977.1:p.Gly4791Ter
XM_011543676.1:c.14293G>T	XP_011541978.1:p.Gly4765Ter
XM_011543677.1:c.11677G>T	XP_011541979.1:p.Gly3893Ter
XM_011543678.1:c.14374G>T	XP_011541980.1:p.Gly4792Ter
NM_032119.4:c.14374G>T MANE Select	NP_115495.3:p.Gly4792Ter
XM_017009963.2:c.14395G>T	XP_016865452.1:p.Gly4799Ter
XM_017009964.2:c.14392G>T	XP_016865453.1:p.Gly4798Ter
XM_017009965.1:c.14392G>T	XP_016865454.1:p.Gly4798Ter
XM_017009966.2:c.14314G>T	XP_016865455.1:p.Gly4772Ter
XM_017009967.1:c.14299G>T	XP_016865456.1:p.Gly4767Ter
XM_017009968.2:c.14395G>T	XP_016865457.1:p.Gly4799Ter
XM_017009969.2:c.14395G>T	XP_016865458.1:p.Gly4799Ter
XM_017009970.2:c.14395G>T	XP_016865459.1:p.Gly4799Ter
XM_017009971.2:c.14395G>T	XP_016865460.1:p.Gly4799Ter
XM_017009972.1:c.7513G>T	XP_016865461.1:p.Gly2505Ter
XM_017009973.1:c.7492G>T	XP_016865462.1:p.Gly2498Ter
NR_003149.2:n.14390G>T