Canonical Allele Identifier: CA450411556

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51491892A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627094A>C , CM000668.2:g.51627094A>C	GRCh38
NC_000006.11:g.51491892A>C , CM000668.1:g.51491892A>C	GRCh37
NC_000006.10:g.51599851A>C	NCBI36
NG_008753.1:g.465532T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11688T>G MANE Select	ENSP00000360158.3:p.Pro3896=
ENST00000371117.7:c.11688T>G	ENSP00000360158.3:p.Pro3896=
NM_138694.3:c.11688T>G	NP_619639.3:p.Pro3896=
XM_011514679.1:c.11688T>G	XP_011512981.1:p.Pro3896=
XM_011514680.1:c.11688T>G	XP_011512982.1:p.Pro3896=
XM_011514681.1:c.11559T>G	XP_011512983.1:p.Pro3853=
XM_011514682.1:c.11550T>G	XP_011512984.1:p.Pro3850=
XM_011514683.1:c.11046T>G	XP_011512985.1:p.Pro3682=
XM_011514684.1:c.10977T>G	XP_011512986.1:p.Pro3659=
XM_011514690.1:c.5763T>G	XP_011512992.1:p.Pro1921=
XM_011514691.1:c.5763T>G	XP_011512993.1:p.Pro1921=
XM_011514680.3:c.11688T>G	XP_011512982.1:p.Pro3896=
XM_011514682.3:c.11550T>G	XP_011512984.1:p.Pro3850=
XM_011514683.3:c.11046T>G	XP_011512985.1:p.Pro3682=
XM_011514684.3:c.10977T>G	XP_011512986.1:p.Pro3659=
XM_011514690.3:c.5763T>G	XP_011512992.1:p.Pro1921=
XM_011514691.3:c.5763T>G	XP_011512993.1:p.Pro1921=
XM_017010944.2:c.11688T>G	XP_016866433.1:p.Pro3896=
XM_017010945.2:c.11613T>G	XP_016866434.1:p.Pro3871=
XM_017010946.2:c.11493T>G	XP_016866435.1:p.Pro3831=
XM_017010947.2:c.11424T>G	XP_016866436.1:p.Pro3808=
XM_017010948.2:c.10977T>G	XP_016866437.1:p.Pro3659=
XM_017010949.2:c.9828T>G	XP_016866438.1:p.Pro3276=
NM_138694.4:c.11688T>G MANE Select	NP_619639.3:p.Pro3896=