Canonical Allele Identifier: CA450412549

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51618018G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51753220G>C , CM000668.2:g.51753220G>C	GRCh38
NC_000006.11:g.51618018G>C , CM000668.1:g.51618018G>C	GRCh37
NC_000006.10:g.51725977G>C	NCBI36
NG_008753.1:g.339406C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.8931C>G MANE Select	ENSP00000360158.3:p.Ser2977=
ENST00000340994.4:c.8931C>G	ENSP00000341097.4:p.Ser2977=
ENST00000371117.7:c.8931C>G	ENSP00000360158.3:p.Ser2977=
NM_138694.3:c.8931C>G	NP_619639.3:p.Ser2977=
NM_170724.2:c.8931C>G	NP_733842.2:p.Ser2977=
XM_011514679.1:c.8931C>G	XP_011512981.1:p.Ser2977=
XM_011514680.1:c.8931C>G	XP_011512982.1:p.Ser2977=
XM_011514681.1:c.8802C>G	XP_011512983.1:p.Ser2934=
XM_011514682.1:c.8793C>G	XP_011512984.1:p.Ser2931=
XM_011514683.1:c.8289C>G	XP_011512985.1:p.Ser2763=
XM_011514684.1:c.8220C>G	XP_011512986.1:p.Ser2740=
XM_011514685.1:c.8931C>G	XP_011512987.1:p.Ser2977=
XM_011514686.1:c.8931C>G	XP_011512988.1:p.Ser2977=
XM_011514687.1:c.8931C>G	XP_011512989.1:p.Ser2977=
XM_011514688.1:c.8931C>G	XP_011512990.1:p.Ser2977=
XM_011514690.1:c.3006C>G	XP_011512992.1:p.Ser1002=
XM_011514691.1:c.3006C>G	XP_011512993.1:p.Ser1002=
XM_011514680.3:c.8931C>G	XP_011512982.1:p.Ser2977=
XM_011514682.3:c.8793C>G	XP_011512984.1:p.Ser2931=
XM_011514683.3:c.8289C>G	XP_011512985.1:p.Ser2763=
XM_011514684.3:c.8220C>G	XP_011512986.1:p.Ser2740=
XM_011514686.2:c.8931C>G	XP_011512988.1:p.Ser2977=
XM_011514688.2:c.8931C>G	XP_011512990.1:p.Ser2977=
XM_011514690.3:c.3006C>G	XP_011512992.1:p.Ser1002=
XM_011514691.3:c.3006C>G	XP_011512993.1:p.Ser1002=
XM_017010944.2:c.8931C>G	XP_016866433.1:p.Ser2977=
XM_017010945.2:c.8856C>G	XP_016866434.1:p.Ser2952=
XM_017010946.2:c.8736C>G	XP_016866435.1:p.Ser2912=
XM_017010947.2:c.8667C>G	XP_016866436.1:p.Ser2889=
XM_017010948.2:c.8220C>G	XP_016866437.1:p.Ser2740=
XM_017010949.2:c.7071C>G	XP_016866438.1:p.Ser2357=
XM_017010950.1:c.8931C>G	XP_016866439.1:p.Ser2977=
XR_001743469.1:n.9207C>G
NM_138694.4:c.8931C>G MANE Select	NP_619639.3:p.Ser2977=
NM_170724.3:c.8931C>G	NP_733842.2:p.Ser2977=