Canonical Allele Identifier: CA11120877

Gene: CNNM4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96762583G>A , CM000664.2:g.96762583G>A	GRCh38
NC_000002.11:g.97428320G>A , CM000664.1:g.97428320G>A	GRCh37
NC_000002.10:g.96792047G>A	NCBI36
NG_016608.1:g.6682G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020184.4:c.1402+182G>A MANE Select	NP_064569.3:n.1402+182G>A
ENST00000377075.3:c.1402+182G>A MANE Select	ENSP00000366275.2:n.1402+182G>A
NM_020184.3:c.1402+182G>A	NP_064569.3:n.1402+182G>A
ENST00000377075.2:c.1402+182G>A	ENSP00000366275.2:n.1402+182G>A
XM_005263914.2:c.1402+182G>A	XP_005263971.1:n.1402+182G>A
XM_005263914.4:c.1402+182G>A	XP_005263971.1:n.1402+182G>A
XM_005263915.2:c.1402+182G>A	XP_005263972.1:n.1402+182G>A
XM_005263915.4:c.1402+182G>A	XP_005263972.1:n.1402+182G>A
XM_011510955.1:c.1402+182G>A	XP_011509257.1:n.1402+182G>A
XM_011510955.3:c.1402+182G>A	XP_011509257.1:n.1402+182G>A
XM_011510956.1:c.1402+182G>A	XP_011509258.1:n.1402+182G>A
XM_011510956.3:c.1402+182G>A	XP_011509258.1:n.1402+182G>A