Canonical Allele Identifier: CA364421249

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51613047C>G (hg19) ; chr6:g.51748249C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51748249C>G , CM000668.2:g.51748249C>G	GRCh38
NC_000006.11:g.51613047C>G , CM000668.1:g.51613047C>G	GRCh37
NC_000006.10:g.51721006C>G	NCBI36
NG_008753.1:g.344377G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.9367G>C MANE Select	ENSP00000360158.3:p.Ala3123Pro
ENST00000340994.4:c.9367G>C	ENSP00000341097.4:p.Ala3123Pro
ENST00000371117.7:c.9367G>C	ENSP00000360158.3:p.Ala3123Pro
NM_138694.3:c.9367G>C	NP_619639.3:p.Ala3123Pro
NM_170724.2:c.9367G>C	NP_733842.2:p.Ala3123Pro
XM_011514679.1:c.9367G>C	XP_011512981.1:p.Ala3123Pro
XM_011514680.1:c.9367G>C	XP_011512982.1:p.Ala3123Pro
XM_011514681.1:c.9238G>C	XP_011512983.1:p.Ala3080Pro
XM_011514682.1:c.9229G>C	XP_011512984.1:p.Ala3077Pro
XM_011514683.1:c.8725G>C	XP_011512985.1:p.Ala2909Pro
XM_011514684.1:c.8656G>C	XP_011512986.1:p.Ala2886Pro
XM_011514685.1:c.9367G>C	XP_011512987.1:p.Ala3123Pro
XM_011514686.1:c.9367G>C	XP_011512988.1:p.Ala3123Pro
XM_011514687.1:c.9367G>C	XP_011512989.1:p.Ala3123Pro
XM_011514688.1:c.9367G>C	XP_011512990.1:p.Ala3123Pro
XM_011514690.1:c.3442G>C	XP_011512992.1:p.Ala1148Pro
XM_011514691.1:c.3442G>C	XP_011512993.1:p.Ala1148Pro
XM_011514680.3:c.9367G>C	XP_011512982.1:p.Ala3123Pro
XM_011514682.3:c.9229G>C	XP_011512984.1:p.Ala3077Pro
XM_011514683.3:c.8725G>C	XP_011512985.1:p.Ala2909Pro
XM_011514684.3:c.8656G>C	XP_011512986.1:p.Ala2886Pro
XM_011514686.2:c.9367G>C	XP_011512988.1:p.Ala3123Pro
XM_011514688.2:c.9367G>C	XP_011512990.1:p.Ala3123Pro
XM_011514690.3:c.3442G>C	XP_011512992.1:p.Ala1148Pro
XM_011514691.3:c.3442G>C	XP_011512993.1:p.Ala1148Pro
XM_017010944.2:c.9367G>C	XP_016866433.1:p.Ala3123Pro
XM_017010945.2:c.9292G>C	XP_016866434.1:p.Ala3098Pro
XM_017010946.2:c.9172G>C	XP_016866435.1:p.Ala3058Pro
XM_017010947.2:c.9103G>C	XP_016866436.1:p.Ala3035Pro
XM_017010948.2:c.8656G>C	XP_016866437.1:p.Ala2886Pro
XM_017010949.2:c.7507G>C	XP_016866438.1:p.Ala2503Pro
XM_017010950.1:c.9367G>C	XP_016866439.1:p.Ala3123Pro
XR_001743469.1:n.9643G>C
NM_138694.4:c.9367G>C MANE Select	NP_619639.3:p.Ala3123Pro
NM_170724.3:c.9367G>C	NP_733842.2:p.Ala3123Pro