Canonical Allele Identifier: CA394387447

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2164446G>T (hg19) ; chr16:g.2114445G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2114445G>T , CM000678.2:g.2114445G>T	GRCh38
NC_000016.9:g.2164446G>T , CM000678.1:g.2164446G>T	GRCh37
NC_000016.8:g.2104447G>T	NCBI36
NG_008617.1:g.26454C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.2578C>A MANE Select	ENSP00000262304.4:p.Arg860Ser
ENST00000262304.8:c.2578C>A	ENSP00000262304.4:p.Arg860Ser
ENST00000423118.5:c.2578C>A	ENSP00000399501.1:p.Arg860Ser
ENST00000488185.2:c.472+3044C>A
ENST00000565639.6:n.37C>A
ENST00000568591.5:c.1509C>A	ENSP00000457162.1:n.1509C>A
NM_000296.3:c.2578C>A	NP_000287.3:p.Arg860Ser
NM_001009944.2:c.2578C>A	NP_001009944.2:p.Arg860Ser
XM_011522525.1:c.2632C>A	XP_011520827.1:p.Arg878Ser
XM_011522526.1:c.2632C>A	XP_011520828.1:p.Arg878Ser
XM_011522527.1:c.2632C>A	XP_011520829.1:p.Arg878Ser
XM_011522528.1:c.2632C>A	XP_011520830.1:p.Arg878Ser
XM_011522529.1:c.2632C>A	XP_011520831.1:p.Arg878Ser
XM_011522530.1:c.2578C>A	XP_011520832.1:p.Arg860Ser
XM_011522531.1:c.2560C>A	XP_011520833.1:p.Arg854Ser
XM_011522532.1:c.2506C>A	XP_011520834.1:p.Arg836Ser
XM_011522533.1:c.2425C>A	XP_011520835.1:p.Arg809Ser
XM_011522534.1:c.2368C>A	XP_011520836.1:p.Arg790Ser
XM_011522535.1:c.454C>A	XP_011520837.1:p.Arg152Ser
XM_011522536.1:c.2632C>A	XP_011520838.1:p.Arg878Ser
XR_932867.1:n.2647C>A
XR_932868.1:n.2647C>A
XR_932869.1:n.2647C>A
XR_932870.1:n.2647C>A
XM_005255370.3:c.-472C>A	XP_005255427.1:n.-472C>A
XM_011522528.3:c.2632C>A	XP_011520830.1:p.Arg878Ser
XM_011522529.2:c.2632C>A	XP_011520831.1:p.Arg878Ser
XM_024450298.1:c.2578C>A	XP_024306066.1:p.Arg860Ser
XM_024450299.1:c.2506C>A	XP_024306067.1:p.Arg836Ser
XM_024450300.1:c.2368C>A	XP_024306068.1:p.Arg790Ser
XM_024450301.1:c.454C>A	XP_024306069.1:p.Arg152Ser
NM_000296.4:c.2578C>A	NP_000287.4:p.Arg860Ser
NM_001009944.3:c.2578C>A MANE Select	NP_001009944.3:p.Arg860Ser