Canonical Allele Identifier: CA394389487

Gene: PKD1

Linked Data

• gnomAD v4: 16-2115398-C-A
• MyVariant Identifiers: chr16:g.2165399C>A (hg19) ; chr16:g.2115398C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2115398C>A , CM000678.2:g.2115398C>A	GRCh38
NC_000016.9:g.2165399C>A , CM000678.1:g.2165399C>A	GRCh37
NC_000016.8:g.2105400C>A	NCBI36
NG_008617.1:g.25501G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262304.9:c.2077G>T MANE Select	ENSP00000262304.4:p.Gly693Trp
ENST00000262304.8:c.2077G>T	ENSP00000262304.4:p.Gly693Trp
ENST00000423118.5:c.2077G>T	ENSP00000399501.1:p.Gly693Trp
ENST00000488185.2:c.472+2091G>T
ENST00000568591.5:c.1008G>T	ENSP00000457162.1:n.1008G>T
NM_000296.3:c.2077G>T	NP_000287.3:p.Gly693Trp
NM_001009944.2:c.2077G>T	NP_001009944.2:p.Gly693Trp
XM_011522525.1:c.2131G>T	XP_011520827.1:p.Gly711Trp
XM_011522526.1:c.2131G>T	XP_011520828.1:p.Gly711Trp
XM_011522527.1:c.2131G>T	XP_011520829.1:p.Gly711Trp
XM_011522528.1:c.2131G>T	XP_011520830.1:p.Gly711Trp
XM_011522529.1:c.2131G>T	XP_011520831.1:p.Gly711Trp
XM_011522530.1:c.2077G>T	XP_011520832.1:p.Gly693Trp
XM_011522531.1:c.2059G>T	XP_011520833.1:p.Gly687Trp
XM_011522532.1:c.2005G>T	XP_011520834.1:p.Gly669Trp
XM_011522533.1:c.1924G>T	XP_011520835.1:p.Gly642Trp
XM_011522534.1:c.1867G>T	XP_011520836.1:p.Gly623Trp
XM_011522536.1:c.2131G>T	XP_011520838.1:p.Gly711Trp
XR_932867.1:n.2146G>T
XR_932868.1:n.2146G>T
XR_932869.1:n.2146G>T
XR_932870.1:n.2146G>T
XM_011522528.3:c.2131G>T	XP_011520830.1:p.Gly711Trp
XM_011522529.2:c.2131G>T	XP_011520831.1:p.Gly711Trp
XM_024450298.1:c.2077G>T	XP_024306066.1:p.Gly693Trp
XM_024450299.1:c.2005G>T	XP_024306067.1:p.Gly669Trp
XM_024450300.1:c.1867G>T	XP_024306068.1:p.Gly623Trp
NM_000296.4:c.2077G>T	NP_000287.4:p.Gly693Trp
NM_001009944.3:c.2077G>T MANE Select	NP_001009944.3:p.Gly693Trp