Canonical Allele Identifier: CA394371192

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2156653T>G (hg19) ; chr16:g.2106652T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106652T>G , CM000678.2:g.2106652T>G	GRCh38
NC_000016.9:g.2156653T>G , CM000678.1:g.2156653T>G	GRCh37
NC_000016.8:g.2096654T>G	NCBI36
NG_008617.1:g.34247A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7235A>C MANE Select	ENSP00000262304.4:p.Asn2412Thr
ENST00000262304.8:c.7235A>C	ENSP00000262304.4:p.Asn2412Thr
ENST00000415938.7:n.480A>C
ENST00000423118.5:c.7235A>C	ENSP00000399501.1:p.Asn2412Thr
ENST00000483024.1:c.403A>C
ENST00000483558.5:n.294A>C
ENST00000483731.5:n.960A>C
ENST00000486339.6:n.981A>C
ENST00000487932.5:c.1922A>C	ENSP00000457132.1:p.Asn641Thr
ENST00000496574.6:n.1238A>C
ENST00000565639.6:n.943A>C
ENST00000568591.5:c.2396A>C	ENSP00000457162.1:n.2396A>C
ENST00000569983.5:n.591A>C
NM_000296.3:c.7235A>C	NP_000287.3:p.Asn2412Thr
NM_001009944.2:c.7235A>C	NP_001009944.2:p.Asn2412Thr
XM_005255370.2:c.4190A>C	XP_005255427.1:p.Asn1397Thr
XM_011522525.1:c.7313A>C	XP_011520827.1:p.Asn2438Thr
XM_011522526.1:c.7313A>C	XP_011520828.1:p.Asn2438Thr
XM_011522527.1:c.7313A>C	XP_011520829.1:p.Asn2438Thr
XM_011522528.1:c.7289A>C	XP_011520830.1:p.Asn2430Thr
XM_011522529.1:c.7289A>C	XP_011520831.1:p.Asn2430Thr
XM_011522530.1:c.7259A>C	XP_011520832.1:p.Asn2420Thr
XM_011522531.1:c.7241A>C	XP_011520833.1:p.Asn2414Thr
XM_011522532.1:c.7187A>C	XP_011520834.1:p.Asn2396Thr
XM_011522533.1:c.7106A>C	XP_011520835.1:p.Asn2369Thr
XM_011522534.1:c.7049A>C	XP_011520836.1:p.Asn2350Thr
XM_011522535.1:c.5135A>C	XP_011520837.1:p.Asn1712Thr
XM_011522536.1:c.7313A>C	XP_011520838.1:p.Asn2438Thr
XM_011522537.1:c.4313A>C	XP_011520839.1:p.Asn1438Thr
XR_932867.1:n.7328A>C
XR_932868.1:n.7328A>C
XR_932869.1:n.7328A>C
XR_932870.1:n.7328A>C
XM_005255370.3:c.4190A>C	XP_005255427.1:p.Asn1397Thr
XM_011522528.3:c.7289A>C	XP_011520830.1:p.Asn2430Thr
XM_011522529.2:c.7289A>C	XP_011520831.1:p.Asn2430Thr
XM_011522537.2:c.4313A>C	XP_011520839.1:p.Asn1438Thr
XM_024450298.1:c.7355A>C	XP_024306066.1:p.Asn2452Thr
XM_024450299.1:c.7283A>C	XP_024306067.1:p.Asn2428Thr
XM_024450300.1:c.7145A>C	XP_024306068.1:p.Asn2382Thr
XM_024450301.1:c.5231A>C	XP_024306069.1:p.Asn1744Thr
NM_000296.4:c.7235A>C	NP_000287.4:p.Asn2412Thr
NM_001009944.3:c.7235A>C MANE Select	NP_001009944.3:p.Asn2412Thr