Canonical Allele Identifier: CA364421014

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51612954C>A (hg19) ; chr6:g.51748156C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51748156C>A , CM000668.2:g.51748156C>A	GRCh38
NC_000006.11:g.51612954C>A , CM000668.1:g.51612954C>A	GRCh37
NC_000006.10:g.51720913C>A	NCBI36
NG_008753.1:g.344470G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.9460G>T MANE Select	ENSP00000360158.3:p.Asp3154Tyr
ENST00000340994.4:c.9460G>T	ENSP00000341097.4:p.Asp3154Tyr
ENST00000371117.7:c.9460G>T	ENSP00000360158.3:p.Asp3154Tyr
NM_138694.3:c.9460G>T	NP_619639.3:p.Asp3154Tyr
NM_170724.2:c.9460G>T	NP_733842.2:p.Asp3154Tyr
XM_011514679.1:c.9460G>T	XP_011512981.1:p.Asp3154Tyr
XM_011514680.1:c.9460G>T	XP_011512982.1:p.Asp3154Tyr
XM_011514681.1:c.9331G>T	XP_011512983.1:p.Asp3111Tyr
XM_011514682.1:c.9322G>T	XP_011512984.1:p.Asp3108Tyr
XM_011514683.1:c.8818G>T	XP_011512985.1:p.Asp2940Tyr
XM_011514684.1:c.8749G>T	XP_011512986.1:p.Asp2917Tyr
XM_011514685.1:c.9460G>T	XP_011512987.1:p.Asp3154Tyr
XM_011514686.1:c.9460G>T	XP_011512988.1:p.Asp3154Tyr
XM_011514687.1:c.9460G>T	XP_011512989.1:p.Asp3154Tyr
XM_011514688.1:c.9460G>T	XP_011512990.1:p.Asp3154Tyr
XM_011514690.1:c.3535G>T	XP_011512992.1:p.Asp1179Tyr
XM_011514691.1:c.3535G>T	XP_011512993.1:p.Asp1179Tyr
XM_011514680.3:c.9460G>T	XP_011512982.1:p.Asp3154Tyr
XM_011514682.3:c.9322G>T	XP_011512984.1:p.Asp3108Tyr
XM_011514683.3:c.8818G>T	XP_011512985.1:p.Asp2940Tyr
XM_011514684.3:c.8749G>T	XP_011512986.1:p.Asp2917Tyr
XM_011514686.2:c.9460G>T	XP_011512988.1:p.Asp3154Tyr
XM_011514688.2:c.9460G>T	XP_011512990.1:p.Asp3154Tyr
XM_011514690.3:c.3535G>T	XP_011512992.1:p.Asp1179Tyr
XM_011514691.3:c.3535G>T	XP_011512993.1:p.Asp1179Tyr
XM_017010944.2:c.9460G>T	XP_016866433.1:p.Asp3154Tyr
XM_017010945.2:c.9385G>T	XP_016866434.1:p.Asp3129Tyr
XM_017010946.2:c.9265G>T	XP_016866435.1:p.Asp3089Tyr
XM_017010947.2:c.9196G>T	XP_016866436.1:p.Asp3066Tyr
XM_017010948.2:c.8749G>T	XP_016866437.1:p.Asp2917Tyr
XM_017010949.2:c.7600G>T	XP_016866438.1:p.Asp2534Tyr
XM_017010950.1:c.9460G>T	XP_016866439.1:p.Asp3154Tyr
XR_001743469.1:n.9736G>T
NM_138694.4:c.9460G>T MANE Select	NP_619639.3:p.Asp3154Tyr
NM_170724.3:c.9460G>T	NP_733842.2:p.Asp3154Tyr