Canonical Allele Identifier: CA364418822

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51491863T>A (hg19) ; chr6:g.51627065T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627065T>A , CM000668.2:g.51627065T>A	GRCh38
NC_000006.11:g.51491863T>A , CM000668.1:g.51491863T>A	GRCh37
NC_000006.10:g.51599822T>A	NCBI36
NG_008753.1:g.465561A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11717A>T MANE Select	ENSP00000360158.3:p.His3906Leu
ENST00000371117.7:c.11717A>T	ENSP00000360158.3:p.His3906Leu
NM_138694.3:c.11717A>T	NP_619639.3:p.His3906Leu
XM_011514679.1:c.11717A>T	XP_011512981.1:p.His3906Leu
XM_011514680.1:c.11717A>T	XP_011512982.1:p.His3906Leu
XM_011514681.1:c.11588A>T	XP_011512983.1:p.His3863Leu
XM_011514682.1:c.11579A>T	XP_011512984.1:p.His3860Leu
XM_011514683.1:c.11075A>T	XP_011512985.1:p.His3692Leu
XM_011514684.1:c.11006A>T	XP_011512986.1:p.His3669Leu
XM_011514690.1:c.5792A>T	XP_011512992.1:p.His1931Leu
XM_011514691.1:c.5792A>T	XP_011512993.1:p.His1931Leu
XM_011514680.3:c.11717A>T	XP_011512982.1:p.His3906Leu
XM_011514682.3:c.11579A>T	XP_011512984.1:p.His3860Leu
XM_011514683.3:c.11075A>T	XP_011512985.1:p.His3692Leu
XM_011514684.3:c.11006A>T	XP_011512986.1:p.His3669Leu
XM_011514690.3:c.5792A>T	XP_011512992.1:p.His1931Leu
XM_011514691.3:c.5792A>T	XP_011512993.1:p.His1931Leu
XM_017010944.2:c.11717A>T	XP_016866433.1:p.His3906Leu
XM_017010945.2:c.11642A>T	XP_016866434.1:p.His3881Leu
XM_017010946.2:c.11522A>T	XP_016866435.1:p.His3841Leu
XM_017010947.2:c.11453A>T	XP_016866436.1:p.His3818Leu
XM_017010948.2:c.11006A>T	XP_016866437.1:p.His3669Leu
XM_017010949.2:c.9857A>T	XP_016866438.1:p.His3286Leu
NM_138694.4:c.11717A>T MANE Select	NP_619639.3:p.His3906Leu