Canonical Allele Identifier: CA364424123

Gene: PKHD1

Linked Data

• COSMIC: COSM5771107 ; COSM5771108
• MyVariant Identifiers: chr6:g.51613382G>A (hg19) ; chr6:g.51748584G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51748584G>A , CM000668.2:g.51748584G>A	GRCh38
NC_000006.11:g.51613382G>A , CM000668.1:g.51613382G>A	GRCh37
NC_000006.10:g.51721341G>A	NCBI36
NG_008753.1:g.344042C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.9032C>T MANE Select	ENSP00000360158.3:p.Ala3011Val
ENST00000340994.4:c.9032C>T	ENSP00000341097.4:p.Ala3011Val
ENST00000371117.7:c.9032C>T	ENSP00000360158.3:p.Ala3011Val
NM_138694.3:c.9032C>T	NP_619639.3:p.Ala3011Val
NM_170724.2:c.9032C>T	NP_733842.2:p.Ala3011Val
XM_011514679.1:c.9032C>T	XP_011512981.1:p.Ala3011Val
XM_011514680.1:c.9032C>T	XP_011512982.1:p.Ala3011Val
XM_011514681.1:c.8903C>T	XP_011512983.1:p.Ala2968Val
XM_011514682.1:c.8894C>T	XP_011512984.1:p.Ala2965Val
XM_011514683.1:c.8390C>T	XP_011512985.1:p.Ala2797Val
XM_011514684.1:c.8321C>T	XP_011512986.1:p.Ala2774Val
XM_011514685.1:c.9032C>T	XP_011512987.1:p.Ala3011Val
XM_011514686.1:c.9032C>T	XP_011512988.1:p.Ala3011Val
XM_011514687.1:c.9032C>T	XP_011512989.1:p.Ala3011Val
XM_011514688.1:c.9032C>T	XP_011512990.1:p.Ala3011Val
XM_011514690.1:c.3107C>T	XP_011512992.1:p.Ala1036Val
XM_011514691.1:c.3107C>T	XP_011512993.1:p.Ala1036Val
XM_011514680.3:c.9032C>T	XP_011512982.1:p.Ala3011Val
XM_011514682.3:c.8894C>T	XP_011512984.1:p.Ala2965Val
XM_011514683.3:c.8390C>T	XP_011512985.1:p.Ala2797Val
XM_011514684.3:c.8321C>T	XP_011512986.1:p.Ala2774Val
XM_011514686.2:c.9032C>T	XP_011512988.1:p.Ala3011Val
XM_011514688.2:c.9032C>T	XP_011512990.1:p.Ala3011Val
XM_011514690.3:c.3107C>T	XP_011512992.1:p.Ala1036Val
XM_011514691.3:c.3107C>T	XP_011512993.1:p.Ala1036Val
XM_017010944.2:c.9032C>T	XP_016866433.1:p.Ala3011Val
XM_017010945.2:c.8957C>T	XP_016866434.1:p.Ala2986Val
XM_017010946.2:c.8837C>T	XP_016866435.1:p.Ala2946Val
XM_017010947.2:c.8768C>T	XP_016866436.1:p.Ala2923Val
XM_017010948.2:c.8321C>T	XP_016866437.1:p.Ala2774Val
XM_017010949.2:c.7172C>T	XP_016866438.1:p.Ala2391Val
XM_017010950.1:c.9032C>T	XP_016866439.1:p.Ala3011Val
XR_001743469.1:n.9308C>T
NM_138694.4:c.9032C>T MANE Select	NP_619639.3:p.Ala3011Val
NM_170724.3:c.9032C>T	NP_733842.2:p.Ala3011Val