Canonical Allele Identifier: CA360407541

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90040889A>C (hg19) ; chr5:g.90745072A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745072A>C , CM000667.2:g.90745072A>C	GRCh38
NC_000005.9:g.90040889A>C , CM000667.1:g.90040889A>C	GRCh37
NC_000005.8:g.90076645A>C	NCBI36
NG_007083.1:g.191273A>C
NG_007083.2:g.220729A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10576A>C MANE Select	ENSP00000384582.2:p.Met3526Leu
ENST00000639431.1:c.265+68863A>C	ENSP00000491057.1:n.265+68863A>C
ENST00000640374.1:n.3720A>C
ENST00000640464.1:n.995A>C
ENST00000405460.6:c.10576A>C	ENSP00000384582.2:p.Met3526Leu
ENST00000509621.1:c.3273A>C
NM_032119.3:c.10576A>C	NP_115495.3:p.Met3526Leu
NR_003149.1:n.10589A>C
XM_011543675.1:c.10573A>C	XP_011541977.1:p.Met3525Leu
XM_011543676.1:c.10495A>C	XP_011541978.1:p.Met3499Leu
XM_011543677.1:c.7879A>C	XP_011541979.1:p.Met2627Leu
XM_011543678.1:c.10576A>C	XP_011541980.1:p.Met3526Leu
XM_011543679.1:c.10576A>C	XP_011541981.1:p.Met3526Leu
NM_032119.4:c.10576A>C MANE Select	NP_115495.3:p.Met3526Leu
XM_017009963.2:c.10597A>C	XP_016865452.1:p.Met3533Leu
XM_017009964.2:c.10594A>C	XP_016865453.1:p.Met3532Leu
XM_017009965.1:c.10594A>C	XP_016865454.1:p.Met3532Leu
XM_017009966.2:c.10516A>C	XP_016865455.1:p.Met3506Leu
XM_017009967.1:c.10501A>C	XP_016865456.1:p.Met3501Leu
XM_017009968.2:c.10597A>C	XP_016865457.1:p.Met3533Leu
XM_017009969.2:c.10597A>C	XP_016865458.1:p.Met3533Leu
XM_017009970.2:c.10597A>C	XP_016865459.1:p.Met3533Leu
XM_017009971.2:c.10597A>C	XP_016865460.1:p.Met3533Leu
XM_017009972.1:c.3715A>C	XP_016865461.1:p.Met1239Leu
XM_017009973.1:c.3694A>C	XP_016865462.1:p.Met1232Leu
XM_017009974.2:c.10597A>C	XP_016865463.1:p.Met3533Leu
NR_003149.2:n.10592A>C