Canonical Allele Identifier: CA138875910

Gene: PKHD1

Linked Data

• dbSNP Id: rs558283274
• gnomAD v3: 6-51627059-T-C
• gnomAD v4: 6-51627059-T-C
• MyVariant Identifiers: chr6:g.51491857T>C (hg19) ; chr6:g.51627059T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627059T>C , CM000668.2:g.51627059T>C	GRCh38
NC_000006.11:g.51491857T>C , CM000668.1:g.51491857T>C	GRCh37
NC_000006.10:g.51599816T>C	NCBI36
NG_008753.1:g.465567A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11723A>G MANE Select	ENSP00000360158.3:p.His3908Arg
ENST00000371117.7:c.11723A>G	ENSP00000360158.3:p.His3908Arg
NM_138694.3:c.11723A>G	NP_619639.3:p.His3908Arg
XM_011514679.1:c.11723A>G	XP_011512981.1:p.His3908Arg
XM_011514680.1:c.11723A>G	XP_011512982.1:p.His3908Arg
XM_011514681.1:c.11594A>G	XP_011512983.1:p.His3865Arg
XM_011514682.1:c.11585A>G	XP_011512984.1:p.His3862Arg
XM_011514683.1:c.11081A>G	XP_011512985.1:p.His3694Arg
XM_011514684.1:c.11012A>G	XP_011512986.1:p.His3671Arg
XM_011514690.1:c.5798A>G	XP_011512992.1:p.His1933Arg
XM_011514691.1:c.5798A>G	XP_011512993.1:p.His1933Arg
XM_011514680.3:c.11723A>G	XP_011512982.1:p.His3908Arg
XM_011514682.3:c.11585A>G	XP_011512984.1:p.His3862Arg
XM_011514683.3:c.11081A>G	XP_011512985.1:p.His3694Arg
XM_011514684.3:c.11012A>G	XP_011512986.1:p.His3671Arg
XM_011514690.3:c.5798A>G	XP_011512992.1:p.His1933Arg
XM_011514691.3:c.5798A>G	XP_011512993.1:p.His1933Arg
XM_017010944.2:c.11723A>G	XP_016866433.1:p.His3908Arg
XM_017010945.2:c.11648A>G	XP_016866434.1:p.His3883Arg
XM_017010946.2:c.11528A>G	XP_016866435.1:p.His3843Arg
XM_017010947.2:c.11459A>G	XP_016866436.1:p.His3820Arg
XM_017010948.2:c.11012A>G	XP_016866437.1:p.His3671Arg
XM_017010949.2:c.9863A>G	XP_016866438.1:p.His3288Arg
NM_138694.4:c.11723A>G MANE Select	NP_619639.3:p.His3908Arg