Canonical Allele Identifier: CA450613744

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51613276T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51748478T>C , CM000668.2:g.51748478T>C	GRCh38
NC_000006.11:g.51613276T>C , CM000668.1:g.51613276T>C	GRCh37
NC_000006.10:g.51721235T>C	NCBI36
NG_008753.1:g.344148A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.9138A>G MANE Select	ENSP00000360158.3:p.Thr3046=
ENST00000340994.4:c.9138A>G	ENSP00000341097.4:p.Thr3046=
ENST00000371117.7:c.9138A>G	ENSP00000360158.3:p.Thr3046=
NM_138694.3:c.9138A>G	NP_619639.3:p.Thr3046=
NM_170724.2:c.9138A>G	NP_733842.2:p.Thr3046=
XM_011514679.1:c.9138A>G	XP_011512981.1:p.Thr3046=
XM_011514680.1:c.9138A>G	XP_011512982.1:p.Thr3046=
XM_011514681.1:c.9009A>G	XP_011512983.1:p.Thr3003=
XM_011514682.1:c.9000A>G	XP_011512984.1:p.Thr3000=
XM_011514683.1:c.8496A>G	XP_011512985.1:p.Thr2832=
XM_011514684.1:c.8427A>G	XP_011512986.1:p.Thr2809=
XM_011514685.1:c.9138A>G	XP_011512987.1:p.Thr3046=
XM_011514686.1:c.9138A>G	XP_011512988.1:p.Thr3046=
XM_011514687.1:c.9138A>G	XP_011512989.1:p.Thr3046=
XM_011514688.1:c.9138A>G	XP_011512990.1:p.Thr3046=
XM_011514690.1:c.3213A>G	XP_011512992.1:p.Thr1071=
XM_011514691.1:c.3213A>G	XP_011512993.1:p.Thr1071=
XM_011514680.3:c.9138A>G	XP_011512982.1:p.Thr3046=
XM_011514682.3:c.9000A>G	XP_011512984.1:p.Thr3000=
XM_011514683.3:c.8496A>G	XP_011512985.1:p.Thr2832=
XM_011514684.3:c.8427A>G	XP_011512986.1:p.Thr2809=
XM_011514686.2:c.9138A>G	XP_011512988.1:p.Thr3046=
XM_011514688.2:c.9138A>G	XP_011512990.1:p.Thr3046=
XM_011514690.3:c.3213A>G	XP_011512992.1:p.Thr1071=
XM_011514691.3:c.3213A>G	XP_011512993.1:p.Thr1071=
XM_017010944.2:c.9138A>G	XP_016866433.1:p.Thr3046=
XM_017010945.2:c.9063A>G	XP_016866434.1:p.Thr3021=
XM_017010946.2:c.8943A>G	XP_016866435.1:p.Thr2981=
XM_017010947.2:c.8874A>G	XP_016866436.1:p.Thr2958=
XM_017010948.2:c.8427A>G	XP_016866437.1:p.Thr2809=
XM_017010949.2:c.7278A>G	XP_016866438.1:p.Thr2426=
XM_017010950.1:c.9138A>G	XP_016866439.1:p.Thr3046=
XR_001743469.1:n.9414A>G
NM_138694.4:c.9138A>G MANE Select	NP_619639.3:p.Thr3046=
NM_170724.3:c.9138A>G	NP_733842.2:p.Thr3046=