Canonical Allele Identifier: CA364421159

Gene: PKHD1

Linked Data

• dbSNP Id: rs753143710
• MyVariant Identifiers: chr6:g.51613016T>G (hg19) ; chr6:g.51748218T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51748218T>G , CM000668.2:g.51748218T>G	GRCh38
NC_000006.11:g.51613016T>G , CM000668.1:g.51613016T>G	GRCh37
NC_000006.10:g.51720975T>G	NCBI36
NG_008753.1:g.344408A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.9398A>C MANE Select	ENSP00000360158.3:p.Tyr3133Ser
ENST00000340994.4:c.9398A>C	ENSP00000341097.4:p.Tyr3133Ser
ENST00000371117.7:c.9398A>C	ENSP00000360158.3:p.Tyr3133Ser
NM_138694.3:c.9398A>C	NP_619639.3:p.Tyr3133Ser
NM_170724.2:c.9398A>C	NP_733842.2:p.Tyr3133Ser
XM_011514679.1:c.9398A>C	XP_011512981.1:p.Tyr3133Ser
XM_011514680.1:c.9398A>C	XP_011512982.1:p.Tyr3133Ser
XM_011514681.1:c.9269A>C	XP_011512983.1:p.Tyr3090Ser
XM_011514682.1:c.9260A>C	XP_011512984.1:p.Tyr3087Ser
XM_011514683.1:c.8756A>C	XP_011512985.1:p.Tyr2919Ser
XM_011514684.1:c.8687A>C	XP_011512986.1:p.Tyr2896Ser
XM_011514685.1:c.9398A>C	XP_011512987.1:p.Tyr3133Ser
XM_011514686.1:c.9398A>C	XP_011512988.1:p.Tyr3133Ser
XM_011514687.1:c.9398A>C	XP_011512989.1:p.Tyr3133Ser
XM_011514688.1:c.9398A>C	XP_011512990.1:p.Tyr3133Ser
XM_011514690.1:c.3473A>C	XP_011512992.1:p.Tyr1158Ser
XM_011514691.1:c.3473A>C	XP_011512993.1:p.Tyr1158Ser
XM_011514680.3:c.9398A>C	XP_011512982.1:p.Tyr3133Ser
XM_011514682.3:c.9260A>C	XP_011512984.1:p.Tyr3087Ser
XM_011514683.3:c.8756A>C	XP_011512985.1:p.Tyr2919Ser
XM_011514684.3:c.8687A>C	XP_011512986.1:p.Tyr2896Ser
XM_011514686.2:c.9398A>C	XP_011512988.1:p.Tyr3133Ser
XM_011514688.2:c.9398A>C	XP_011512990.1:p.Tyr3133Ser
XM_011514690.3:c.3473A>C	XP_011512992.1:p.Tyr1158Ser
XM_011514691.3:c.3473A>C	XP_011512993.1:p.Tyr1158Ser
XM_017010944.2:c.9398A>C	XP_016866433.1:p.Tyr3133Ser
XM_017010945.2:c.9323A>C	XP_016866434.1:p.Tyr3108Ser
XM_017010946.2:c.9203A>C	XP_016866435.1:p.Tyr3068Ser
XM_017010947.2:c.9134A>C	XP_016866436.1:p.Tyr3045Ser
XM_017010948.2:c.8687A>C	XP_016866437.1:p.Tyr2896Ser
XM_017010949.2:c.7538A>C	XP_016866438.1:p.Tyr2513Ser
XM_017010950.1:c.9398A>C	XP_016866439.1:p.Tyr3133Ser
XR_001743469.1:n.9674A>C
NM_138694.4:c.9398A>C MANE Select	NP_619639.3:p.Tyr3133Ser
NM_170724.3:c.9398A>C	NP_733842.2:p.Tyr3133Ser