Canonical Allele Identifier: CA247878
Community Standard Title: NM_032119.4(ADGRV1):c.17669T>A (p.Met5890Lys)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90855815T>A , CM000667.2:g.90855815T>A GRCh38
NC_000005.9:g.90151632T>A , CM000667.1:g.90151632T>A GRCh37
NC_000005.8:g.90187388T>A NCBI36
NG_007083.1:g.302016T>A
NG_007083.2:g.331472T>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.17669T>A MANE Select NP_115495.3:p.Met5890Lys
ENST00000405460.9:c.17669T>A MANE Select ENSP00000384582.2:p.Met5890Lys
NM_032119.3:c.17669T>A NP_115495.3:p.Met5890Lys
NR_003149.1:n.17682T>A
NR_003149.2:n.17685T>A
ENST00000405460.6:c.17669T>A ENSP00000384582.2:p.Met5890Lys
ENST00000425867.2:c.4652T>A ENSP00000392618.2:p.Met1551Lys
ENST00000425867.3:c.6623T>A ENSP00000392618.3:p.Met2208Lys
ENST00000503852.1:n.217T>A
ENST00000638510.1:n.4936T>A
ENST00000638990.1:c.881T>A
ENST00000639431.1:c.266-129529T>A ENSP00000491057.1:n.266-129529T>A
ENST00000640407.1:c.4118T>A ENSP00000491425.1:n.4118T>A
XM_011543675.1:c.17666T>A XP_011541977.1:p.Met5889Lys
XM_011543676.1:c.17588T>A XP_011541978.1:p.Met5863Lys
XM_011543677.1:c.14972T>A XP_011541979.1:p.Met4991Lys
XM_017009963.2:c.17690T>A XP_016865452.1:p.Met5897Lys
XM_017009964.2:c.17687T>A XP_016865453.1:p.Met5896Lys
XM_017009965.1:c.17687T>A XP_016865454.1:p.Met5896Lys
XM_017009966.2:c.17609T>A XP_016865455.1:p.Met5870Lys
XM_017009967.1:c.17594T>A XP_016865456.1:p.Met5865Lys
XM_017009968.2:c.17510T>A XP_016865457.1:p.Met5837Lys
XM_017009969.2:c.17690T>A XP_016865458.1:p.Met5897Lys
XM_017009972.1:c.10808T>A XP_016865461.1:p.Met3603Lys
XM_017009973.1:c.10787T>A XP_016865462.1:p.Met3596Lys