Canonical Allele Identifier: CA364418947

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51491896A>G (hg19) ; chr6:g.51627098A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627098A>G , CM000668.2:g.51627098A>G	GRCh38
NC_000006.11:g.51491896A>G , CM000668.1:g.51491896A>G	GRCh37
NC_000006.10:g.51599855A>G	NCBI36
NG_008753.1:g.465528T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11684T>C MANE Select	ENSP00000360158.3:p.Ile3895Thr
ENST00000371117.7:c.11684T>C	ENSP00000360158.3:p.Ile3895Thr
NM_138694.3:c.11684T>C	NP_619639.3:p.Ile3895Thr
XM_011514679.1:c.11684T>C	XP_011512981.1:p.Ile3895Thr
XM_011514680.1:c.11684T>C	XP_011512982.1:p.Ile3895Thr
XM_011514681.1:c.11555T>C	XP_011512983.1:p.Ile3852Thr
XM_011514682.1:c.11546T>C	XP_011512984.1:p.Ile3849Thr
XM_011514683.1:c.11042T>C	XP_011512985.1:p.Ile3681Thr
XM_011514684.1:c.10973T>C	XP_011512986.1:p.Ile3658Thr
XM_011514690.1:c.5759T>C	XP_011512992.1:p.Ile1920Thr
XM_011514691.1:c.5759T>C	XP_011512993.1:p.Ile1920Thr
XM_011514680.3:c.11684T>C	XP_011512982.1:p.Ile3895Thr
XM_011514682.3:c.11546T>C	XP_011512984.1:p.Ile3849Thr
XM_011514683.3:c.11042T>C	XP_011512985.1:p.Ile3681Thr
XM_011514684.3:c.10973T>C	XP_011512986.1:p.Ile3658Thr
XM_011514690.3:c.5759T>C	XP_011512992.1:p.Ile1920Thr
XM_011514691.3:c.5759T>C	XP_011512993.1:p.Ile1920Thr
XM_017010944.2:c.11684T>C	XP_016866433.1:p.Ile3895Thr
XM_017010945.2:c.11609T>C	XP_016866434.1:p.Ile3870Thr
XM_017010946.2:c.11489T>C	XP_016866435.1:p.Ile3830Thr
XM_017010947.2:c.11420T>C	XP_016866436.1:p.Ile3807Thr
XM_017010948.2:c.10973T>C	XP_016866437.1:p.Ile3658Thr
XM_017010949.2:c.9824T>C	XP_016866438.1:p.Ile3275Thr
NM_138694.4:c.11684T>C MANE Select	NP_619639.3:p.Ile3895Thr