Canonical Allele Identifier: CA364423814
Community Standard Title: NM_138694.4(PKHD1):c.8208G>A (p.Trp2736Ter)
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51830955C>T , CM000668.2:g.51830955C>T GRCh38
NC_000006.11:g.51695753C>T , CM000668.1:g.51695753C>T GRCh37
NC_000006.10:g.51803712C>T NCBI36
NG_008753.1:g.261671G>A

Transcript Alleles

HGVS Amino-acid Change
NM_138694.4:c.8208G>A MANE Select NP_619639.3:p.Trp2736Ter
ENST00000371117.8:c.8208G>A MANE Select ENSP00000360158.3:p.Trp2736Ter
NM_138694.3:c.8208G>A NP_619639.3:p.Trp2736Ter
NM_170724.2:c.8208G>A NP_733842.2:p.Trp2736Ter
NM_170724.3:c.8208G>A NP_733842.2:p.Trp2736Ter
ENST00000340994.4:c.8208G>A ENSP00000341097.4:p.Trp2736Ter
ENST00000371117.7:c.8208G>A ENSP00000360158.3:p.Trp2736Ter
XM_011514679.1:c.8208G>A XP_011512981.1:p.Trp2736Ter
XM_011514680.1:c.8208G>A XP_011512982.1:p.Trp2736Ter
XM_011514680.3:c.8208G>A XP_011512982.1:p.Trp2736Ter
XM_011514681.1:c.8173+5449G>A XP_011512983.1:n.8173+5449G>A
XM_011514682.1:c.8208G>A XP_011512984.1:p.Trp2736Ter
XM_011514682.3:c.8208G>A XP_011512984.1:p.Trp2736Ter
XM_011514683.1:c.7566G>A XP_011512985.1:p.Trp2522Ter
XM_011514683.3:c.7566G>A XP_011512985.1:p.Trp2522Ter
XM_011514684.1:c.7497G>A XP_011512986.1:p.Trp2499Ter
XM_011514684.3:c.7497G>A XP_011512986.1:p.Trp2499Ter
XM_011514685.1:c.8208G>A XP_011512987.1:p.Trp2736Ter
XM_011514686.1:c.8208G>A XP_011512988.1:p.Trp2736Ter
XM_011514686.2:c.8208G>A XP_011512988.1:p.Trp2736Ter
XM_011514687.1:c.8208G>A XP_011512989.1:p.Trp2736Ter
XM_011514688.1:c.8208G>A XP_011512990.1:p.Trp2736Ter
XM_011514688.2:c.8208G>A XP_011512990.1:p.Trp2736Ter
XM_011514689.1:c.8208G>A XP_011512991.1:p.Trp2736Ter
XM_011514690.1:c.2283G>A XP_011512992.1:p.Trp761Ter
XM_011514690.3:c.2283G>A XP_011512992.1:p.Trp761Ter
XM_011514691.1:c.2283G>A XP_011512993.1:p.Trp761Ter
XM_011514691.3:c.2283G>A XP_011512993.1:p.Trp761Ter
XM_017010944.2:c.8208G>A XP_016866433.1:p.Trp2736Ter
XM_017010945.2:c.8133G>A XP_016866434.1:p.Trp2711Ter
XM_017010946.2:c.8107+16820G>A XP_016866435.1:n.8107+16820G>A
XM_017010947.2:c.7944G>A XP_016866436.1:p.Trp2648Ter
XM_017010948.2:c.7497G>A XP_016866437.1:p.Trp2499Ter
XM_017010949.2:c.6348G>A XP_016866438.1:p.Trp2116Ter
XM_017010950.1:c.8208G>A XP_016866439.1:p.Trp2736Ter
XM_017010951.1:c.8208G>A XP_016866440.1:p.Trp2736Ter
XM_017010952.1:c.8208G>A XP_016866441.1:p.Trp2736Ter
XR_001743469.1:n.8484G>A