Canonical Allele Identifier: CA156511679

Linked Data

dbSNP Id: rs79977919

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.29144776G>C , CM000669.2:g.29144776G>C GRCh38
NC_000007.13:g.29184392G>C , CM000669.1:g.29184392G>C GRCh37
NC_000007.12:g.29150917G>C NCBI36
NG_029365.2:g.3230G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000265394.10:c.-11+1653C>G (CPVL) MANE Select ENSP00000265394.5:n.-11+1653C>G
ENST00000644824.1:c.-730-1078G>C ENSP00000495614.1:n.-730-1078G>C
ENST00000265394.9:c.-11+1653C>G (CPVL) ENSP00000265394.5:n.-11+1653C>G
ENST00000396276.7:c.-11+1565C>G (CPVL) ENSP00000379572.3:n.-11+1565C>G
ENST00000409850.5:c.-10-23705C>G (CPVL) ENSP00000387164.1:n.-10-23705C>G
ENST00000423511.1:c.-730-1078G>C (CHN2) ENSP00000462650.1:n.-730-1078G>C
ENST00000437527.1:c.-10-23705C>G (CPVL) ENSP00000416555.1:n.-10-23705C>G
ENST00000449801.5:c.-10-23705C>G (CPVL) ENSP00000413287.1:n.-10-23705C>G
ENST00000455544.5:c.-10-23705C>G (CPVL) ENSP00000412857.1:n.-10-23705C>G
ENST00000488891.6:n.284-23705C>G (CPVL)
ENST00000578605.1:n.191-1078G>C (CHN2)
ENST00000612187.4:c.-359+1653C>G (CPVL) ENSP00000479581.1:n.-359+1653C>G
NM_019029.2:c.-11+1565C>G (CPVL) NP_061902.2:n.-11+1565C>G
NM_031311.3:c.-11+1653C>G (CPVL) NP_112601.3:n.-11+1653C>G
XM_011515437.1:c.-11+1345C>G (CPVL) XP_011513739.1:n.-11+1345C>G
NM_001348052.1:c.-10-23705C>G (CPVL) NP_001334981.1:n.-10-23705C>G
NM_001348054.1:c.-10-23705C>G (CPVL) NP_001334983.1:n.-10-23705C>G
NM_019029.3:c.-11+1565C>G (CPVL) NP_061902.2:n.-11+1565C>G
NM_031311.4:c.-11+1653C>G (CPVL) NP_112601.3:n.-11+1653C>G
XM_017012366.1:c.-11+1653C>G (CPVL) XP_016867855.1:n.-11+1653C>G
NM_031311.5:c.-11+1653C>G (CPVL) MANE Select NP_112601.3:n.-11+1653C>G
NM_001371255.1:c.-10-23705C>G (CPVL) NP_001358184.1:n.-10-23705C>G
NM_001371256.1:c.-10-23705C>G (CPVL) NP_001358185.1:n.-10-23705C>G
NM_001371257.1:c.-10-23705C>G (CPVL) NP_001358186.1:n.-10-23705C>G
NM_001371258.1:c.-10-23705C>G (CPVL) NP_001358187.1:n.-10-23705C>G
NM_001371260.1:c.-10-23705C>G (CPVL) NP_001358189.1:n.-10-23705C>G
NM_001371261.1:c.-10-23705C>G (CPVL) NP_001358190.1:n.-10-23705C>G
NM_001371262.1:c.-10-23705C>G (CPVL) NP_001358191.1:n.-10-23705C>G
NM_001371263.1:c.-10-23705C>G (CPVL) NP_001358192.1:n.-10-23705C>G
NM_001371264.1:c.-10-23705C>G (CPVL) NP_001358193.1:n.-10-23705C>G
NM_001371265.1:c.-496-23705C>G (CPVL) NP_001358194.1:n.-496-23705C>G
NM_001371266.1:c.-364-23705C>G (CPVL) NP_001358195.1:n.-364-23705C>G
NM_001371267.1:c.-337-23705C>G (CPVL) NP_001358196.1:n.-337-23705C>G
NM_001371268.1:c.-71-23705C>G (CPVL) NP_001358197.1:n.-71-23705C>G