Canonical Allele Identifier: CA2663153816

Gene: STK36

Linked Data

• gnomAD v4: 2-218680502-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218680502T>C , CM000664.2:g.218680502T>C	GRCh38
NC_000002.11:g.219545225T>C , CM000664.1:g.219545225T>C	GRCh37
NC_000002.10:g.219253469T>C	NCBI36
NG_029739.1:g.13477T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295709.8:c.1137-101T>C MANE Select	ENSP00000295709.3:n.1137-101T>C
ENST00000295709.7:c.1137-101T>C	ENSP00000295709.3:n.1137-101T>C
ENST00000392105.7:c.1137-101T>C	ENSP00000375954.3:n.1137-101T>C
ENST00000414413.5:c.32-101T>C
ENST00000440309.5:c.1137-101T>C	ENSP00000394095.1:n.1137-101T>C
NM_001243313.1:c.1137-101T>C	NP_001230242.1:n.1137-101T>C
NM_015690.4:c.1137-101T>C	NP_056505.2:n.1137-101T>C
XM_005246464.1:c.1137-101T>C	XP_005246521.1:n.1137-101T>C
XM_011510959.1:c.1137-101T>C	XP_011509261.1:n.1137-101T>C
XM_011510960.1:c.975-101T>C	XP_011509262.1:n.975-101T>C
XR_922904.1:n.1416-101T>C
XM_005246464.2:c.1137-101T>C	XP_005246521.1:n.1137-101T>C
XM_011510959.2:c.1137-101T>C	XP_011509261.1:n.1137-101T>C
XM_017003804.2:c.1137-101T>C	XP_016859293.1:n.1137-101T>C
XM_017003805.2:c.-560-101T>C	XP_016859294.1:n.-560-101T>C
XR_001738704.2:n.1393-101T>C
XR_922904.2:n.1393-101T>C
NM_015690.5:c.1137-101T>C MANE Select	NP_056505.2:n.1137-101T>C
NM_001243313.2:c.1137-101T>C	NP_001230242.1:n.1137-101T>C
NM_001369423.1:c.1137-101T>C	NP_001356352.1:n.1137-101T>C