Canonical Allele Identifier: CA364431510

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524053G>C (hg19) ; chr6:g.51659255G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659255G>C , CM000668.2:g.51659255G>C	GRCh38
NC_000006.11:g.51524053G>C , CM000668.1:g.51524053G>C	GRCh37
NC_000006.10:g.51632012G>C	NCBI36
NG_008753.1:g.433371C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10871C>G MANE Select	ENSP00000360158.3:p.Thr3624Ser
ENST00000371117.7:c.10871C>G	ENSP00000360158.3:p.Thr3624Ser
NM_138694.3:c.10871C>G	NP_619639.3:p.Thr3624Ser
XM_011514679.1:c.10871C>G	XP_011512981.1:p.Thr3624Ser
XM_011514680.1:c.10871C>G	XP_011512982.1:p.Thr3624Ser
XM_011514681.1:c.10742C>G	XP_011512983.1:p.Thr3581Ser
XM_011514682.1:c.10733C>G	XP_011512984.1:p.Thr3578Ser
XM_011514683.1:c.10229C>G	XP_011512985.1:p.Thr3410Ser
XM_011514684.1:c.10160C>G	XP_011512986.1:p.Thr3387Ser
XM_011514687.1:c.10157-10035C>G	XP_011512989.1:n.10157-10035C>G
XM_011514690.1:c.4946C>G	XP_011512992.1:p.Thr1649Ser
XM_011514691.1:c.4946C>G	XP_011512993.1:p.Thr1649Ser
XR_926870.1:n.535+6882G>C
XR_926871.1:n.403+6882G>C
XR_926872.1:n.535+6882G>C
XM_011514680.3:c.10871C>G	XP_011512982.1:p.Thr3624Ser
XM_011514682.3:c.10733C>G	XP_011512984.1:p.Thr3578Ser
XM_011514683.3:c.10229C>G	XP_011512985.1:p.Thr3410Ser
XM_011514684.3:c.10160C>G	XP_011512986.1:p.Thr3387Ser
XM_011514690.3:c.4946C>G	XP_011512992.1:p.Thr1649Ser
XM_011514691.3:c.4946C>G	XP_011512993.1:p.Thr1649Ser
XM_017010944.2:c.10871C>G	XP_016866433.1:p.Thr3624Ser
XM_017010945.2:c.10796C>G	XP_016866434.1:p.Thr3599Ser
XM_017010946.2:c.10676C>G	XP_016866435.1:p.Thr3559Ser
XM_017010947.2:c.10607C>G	XP_016866436.1:p.Thr3536Ser
XM_017010948.2:c.10160C>G	XP_016866437.1:p.Thr3387Ser
XM_017010949.2:c.9011C>G	XP_016866438.1:p.Thr3004Ser
XR_001743469.1:n.11147C>G
XR_001744157.1:n.3145+6882G>C
XR_926870.2:n.3145+6882G>C
XR_926871.2:n.3013+6882G>C
XR_926872.2:n.3145+6882G>C
NM_138694.4:c.10871C>G MANE Select	NP_619639.3:p.Thr3624Ser