Canonical Allele Identifier: CA2631134073

Gene: PKD1

Linked Data

• gnomAD v4: 16-2116476-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2116476G>C , CM000678.2:g.2116476G>C	GRCh38
NC_000016.9:g.2166477G>C , CM000678.1:g.2166477G>C	GRCh37
NC_000016.8:g.2106478G>C	NCBI36
NG_008617.1:g.24423C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262304.9:c.1722+53C>G MANE Select	ENSP00000262304.4:n.1722+53C>G
ENST00000262304.8:c.1722+53C>G	ENSP00000262304.4:n.1722+53C>G
ENST00000423118.5:c.1722+53C>G	ENSP00000399501.1:n.1722+53C>G
ENST00000488185.2:c.472+1013C>G
ENST00000568591.5:c.653+53C>G	ENSP00000457162.1:n.653+53C>G
NM_000296.3:c.1722+53C>G	NP_000287.3:n.1722+53C>G
NM_001009944.2:c.1722+53C>G	NP_001009944.2:n.1722+53C>G
XM_011522525.1:c.1776+53C>G	XP_011520827.1:n.1776+53C>G
XM_011522526.1:c.1776+53C>G	XP_011520828.1:n.1776+53C>G
XM_011522527.1:c.1776+53C>G	XP_011520829.1:n.1776+53C>G
XM_011522528.1:c.1776+53C>G	XP_011520830.1:n.1776+53C>G
XM_011522529.1:c.1776+53C>G	XP_011520831.1:n.1776+53C>G
XM_011522530.1:c.1722+53C>G	XP_011520832.1:n.1722+53C>G
XM_011522531.1:c.1704+53C>G	XP_011520833.1:n.1704+53C>G
XM_011522532.1:c.1650+53C>G	XP_011520834.1:n.1650+53C>G
XM_011522533.1:c.1569+53C>G	XP_011520835.1:n.1569+53C>G
XM_011522534.1:c.1512+53C>G	XP_011520836.1:n.1512+53C>G
XM_011522536.1:c.1776+53C>G	XP_011520838.1:n.1776+53C>G
XR_932867.1:n.1791+53C>G
XR_932868.1:n.1791+53C>G
XR_932869.1:n.1791+53C>G
XR_932870.1:n.1791+53C>G
XM_011522528.3:c.1776+53C>G	XP_011520830.1:n.1776+53C>G
XM_011522529.2:c.1776+53C>G	XP_011520831.1:n.1776+53C>G
XM_024450298.1:c.1722+53C>G	XP_024306066.1:n.1722+53C>G
XM_024450299.1:c.1650+53C>G	XP_024306067.1:n.1650+53C>G
XM_024450300.1:c.1512+53C>G	XP_024306068.1:n.1512+53C>G
NM_000296.4:c.1722+53C>G	NP_000287.4:n.1722+53C>G
NM_001009944.3:c.1722+53C>G MANE Select	NP_001009944.3:n.1722+53C>G