Canonical Allele Identifier: CA360429805
Community Standard Title: NM_032119.4(ADGRV1):c.17195C>T (p.Pro5732Leu)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90848812C>T , CM000667.2:g.90848812C>T GRCh38
NC_000005.9:g.90144629C>T , CM000667.1:g.90144629C>T GRCh37
NC_000005.8:g.90180385C>T NCBI36
NG_007083.1:g.295013C>T
NG_007083.2:g.324469C>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.17195C>T MANE Select NP_115495.3:p.Pro5732Leu
ENST00000405460.9:c.17195C>T MANE Select ENSP00000384582.2:p.Pro5732Leu
NM_032119.3:c.17195C>T NP_115495.3:p.Pro5732Leu
NR_003149.1:n.17208C>T
NR_003149.2:n.17211C>T
ENST00000405460.6:c.17195C>T ENSP00000384582.2:p.Pro5732Leu
ENST00000425867.2:c.4178C>T ENSP00000392618.2:p.Pro1393Leu
ENST00000425867.3:c.6149C>T ENSP00000392618.3:p.Pro2050Leu
ENST00000505845.1:n.386C>T
ENST00000505845.2:n.386C>T
ENST00000638510.1:n.4462C>T
ENST00000638990.1:c.216C>T
ENST00000639431.1:c.266-136532C>T ENSP00000491057.1:n.266-136532C>T
ENST00000640407.1:c.3644C>T ENSP00000491425.1:n.3644C>T
XM_011543675.1:c.17192C>T XP_011541977.1:p.Pro5731Leu
XM_011543676.1:c.17114C>T XP_011541978.1:p.Pro5705Leu
XM_011543677.1:c.14498C>T XP_011541979.1:p.Pro4833Leu
XM_017009963.2:c.17216C>T XP_016865452.1:p.Pro5739Leu
XM_017009964.2:c.17213C>T XP_016865453.1:p.Pro5738Leu
XM_017009965.1:c.17213C>T XP_016865454.1:p.Pro5738Leu
XM_017009966.2:c.17135C>T XP_016865455.1:p.Pro5712Leu
XM_017009967.1:c.17120C>T XP_016865456.1:p.Pro5707Leu
XM_017009968.2:c.17036C>T XP_016865457.1:p.Pro5679Leu
XM_017009969.2:c.17216C>T XP_016865458.1:p.Pro5739Leu
XM_017009972.1:c.10334C>T XP_016865461.1:p.Pro3445Leu
XM_017009973.1:c.10313C>T XP_016865462.1:p.Pro3438Leu