Canonical Allele Identifier: CA364439689

Gene: PKHD1

Linked Data

• dbSNP Id: rs1487603082
• gnomAD v2: 6-51777269-A-G
• gnomAD v4: 6-51912471-A-G
• MyVariant Identifiers: chr6:g.51777269A>G (hg19) ; chr6:g.51912471A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51912471A>G , CM000668.2:g.51912471A>G	GRCh38
NC_000006.11:g.51777269A>G , CM000668.1:g.51777269A>G	GRCh37
NC_000006.10:g.51885228A>G	NCBI36
NG_008753.1:g.180155T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.6227T>C MANE Select	ENSP00000360158.3:p.Val2076Ala
ENST00000340994.4:c.6227T>C	ENSP00000341097.4:p.Val2076Ala
ENST00000371117.7:c.6227T>C	ENSP00000360158.3:p.Val2076Ala
NM_138694.3:c.6227T>C	NP_619639.3:p.Val2076Ala
NM_170724.2:c.6227T>C	NP_733842.2:p.Val2076Ala
XM_011514679.1:c.6227T>C	XP_011512981.1:p.Val2076Ala
XM_011514680.1:c.6227T>C	XP_011512982.1:p.Val2076Ala
XM_011514681.1:c.6227T>C	XP_011512983.1:p.Val2076Ala
XM_011514682.1:c.6227T>C	XP_011512984.1:p.Val2076Ala
XM_011514683.1:c.5585T>C	XP_011512985.1:p.Val1862Ala
XM_011514684.1:c.5516T>C	XP_011512986.1:p.Val1839Ala
XM_011514685.1:c.6227T>C	XP_011512987.1:p.Val2076Ala
XM_011514686.1:c.6227T>C	XP_011512988.1:p.Val2076Ala
XM_011514687.1:c.6227T>C	XP_011512989.1:p.Val2076Ala
XM_011514688.1:c.6227T>C	XP_011512990.1:p.Val2076Ala
XM_011514689.1:c.6227T>C	XP_011512991.1:p.Val2076Ala
XM_011514690.1:c.302T>C	XP_011512992.1:p.Val101Ala
XM_011514691.1:c.302T>C	XP_011512993.1:p.Val101Ala
XM_011514680.3:c.6227T>C	XP_011512982.1:p.Val2076Ala
XM_011514682.3:c.6227T>C	XP_011512984.1:p.Val2076Ala
XM_011514683.3:c.5585T>C	XP_011512985.1:p.Val1862Ala
XM_011514684.3:c.5516T>C	XP_011512986.1:p.Val1839Ala
XM_011514686.2:c.6227T>C	XP_011512988.1:p.Val2076Ala
XM_011514688.2:c.6227T>C	XP_011512990.1:p.Val2076Ala
XM_011514690.3:c.302T>C	XP_011512992.1:p.Val101Ala
XM_011514691.3:c.302T>C	XP_011512993.1:p.Val101Ala
XM_017010944.2:c.6227T>C	XP_016866433.1:p.Val2076Ala
XM_017010945.2:c.6152T>C	XP_016866434.1:p.Val2051Ala
XM_017010946.2:c.6227T>C	XP_016866435.1:p.Val2076Ala
XM_017010947.2:c.5963T>C	XP_016866436.1:p.Val1988Ala
XM_017010948.2:c.5516T>C	XP_016866437.1:p.Val1839Ala
XM_017010949.2:c.4367T>C	XP_016866438.1:p.Val1456Ala
XM_017010950.1:c.6227T>C	XP_016866439.1:p.Val2076Ala
XM_017010951.1:c.6227T>C	XP_016866440.1:p.Val2076Ala
XM_017010952.1:c.6227T>C	XP_016866441.1:p.Val2076Ala
XR_001743469.1:n.6503T>C
NM_138694.4:c.6227T>C MANE Select	NP_619639.3:p.Val2076Ala
NM_170724.3:c.6227T>C	NP_733842.2:p.Val2076Ala