Canonical Allele Identifier: CA11135332

Gene: KIAA2012

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202085128G>A , CM000664.2:g.202085128G>A	GRCh38
NC_000002.11:g.202949851G>A , CM000664.1:g.202949851G>A	GRCh37
NC_000002.10:g.202658096G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498697.3:c.370-5642G>A MANE Select	ENSP00000419834.2:n.370-5642G>A
ENST00000409515.3:n.709-5642G>A
ENST00000459709.5:n.877-5642G>A
ENST00000541917.5:c.370-5642G>A	ENSP00000437957.2:n.370-5642G>A
NM_001277372.1:c.370-5642G>A	NP_001264301.1:n.370-5642G>A
XM_006712171.1:c.370-5642G>A	XP_006712234.1:n.370-5642G>A
XM_006712172.1:c.370-5642G>A	XP_006712235.1:n.370-5642G>A
XM_011510467.1:c.370-5642G>A	XP_011508769.1:n.370-5642G>A
XM_011510468.1:c.370-5642G>A	XP_011508770.1:n.370-5642G>A
XR_923794.1:n.85-9562C>T
XR_923795.1:n.614-9562C>T
NM_001277372.2:c.370-5642G>A	NP_001264301.2:n.370-5642G>A
XM_006712172.3:c.370-5642G>A	XP_006712235.1:n.370-5642G>A
XM_017003111.2:c.370-5642G>A	XP_016858600.1:n.370-5642G>A
XM_017003112.2:c.370-5642G>A	XP_016858601.1:n.370-5642G>A
NM_001277372.4:c.370-5642G>A MANE Select	NP_001264301.2:n.370-5642G>A
NM_001367720.2:c.370-5642G>A	NP_001354649.1:n.370-5642G>A