Canonical Allele Identifier: CA364418850

Gene: PKHD1

Linked Data

• dbSNP Id: rs1767335404
• MyVariant Identifiers: chr6:g.51491871T>G (hg19) ; chr6:g.51627073T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627073T>G , CM000668.2:g.51627073T>G	GRCh38
NC_000006.11:g.51491871T>G , CM000668.1:g.51491871T>G	GRCh37
NC_000006.10:g.51599830T>G	NCBI36
NG_008753.1:g.465553A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11709A>C MANE Select	ENSP00000360158.3:p.Gln3903His
ENST00000371117.7:c.11709A>C	ENSP00000360158.3:p.Gln3903His
NM_138694.3:c.11709A>C	NP_619639.3:p.Gln3903His
XM_011514679.1:c.11709A>C	XP_011512981.1:p.Gln3903His
XM_011514680.1:c.11709A>C	XP_011512982.1:p.Gln3903His
XM_011514681.1:c.11580A>C	XP_011512983.1:p.Gln3860His
XM_011514682.1:c.11571A>C	XP_011512984.1:p.Gln3857His
XM_011514683.1:c.11067A>C	XP_011512985.1:p.Gln3689His
XM_011514684.1:c.10998A>C	XP_011512986.1:p.Gln3666His
XM_011514690.1:c.5784A>C	XP_011512992.1:p.Gln1928His
XM_011514691.1:c.5784A>C	XP_011512993.1:p.Gln1928His
XM_011514680.3:c.11709A>C	XP_011512982.1:p.Gln3903His
XM_011514682.3:c.11571A>C	XP_011512984.1:p.Gln3857His
XM_011514683.3:c.11067A>C	XP_011512985.1:p.Gln3689His
XM_011514684.3:c.10998A>C	XP_011512986.1:p.Gln3666His
XM_011514690.3:c.5784A>C	XP_011512992.1:p.Gln1928His
XM_011514691.3:c.5784A>C	XP_011512993.1:p.Gln1928His
XM_017010944.2:c.11709A>C	XP_016866433.1:p.Gln3903His
XM_017010945.2:c.11634A>C	XP_016866434.1:p.Gln3878His
XM_017010946.2:c.11514A>C	XP_016866435.1:p.Gln3838His
XM_017010947.2:c.11445A>C	XP_016866436.1:p.Gln3815His
XM_017010948.2:c.10998A>C	XP_016866437.1:p.Gln3666His
XM_017010949.2:c.9849A>C	XP_016866438.1:p.Gln3283His
NM_138694.4:c.11709A>C MANE Select	NP_619639.3:p.Gln3903His