Canonical Allele Identifier: CA1272753139

Gene: CNNM4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96761467_96761481delinsCGACGGGCCCTGGCT , CM000664.2:g.96761467_96761481delinsCGACGGGCCCTGGCT	GRCh38
NC_000002.11:g.97427204_97427218delinsCGACGGGCCCTGGCT , CM000664.1:g.97427204_97427218delinsCGACGGGCCCTGGCT	GRCh37
NC_000002.10:g.96790931_96790945delinsCGACGGGCCCTGGCT	NCBI36
NG_016608.1:g.5566_5580delinsCGACGGGCCCTGGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.468_482delinsCGACGGGCCCTGGCT MANE Select	ENSP00000366275.2:p.Pro156=
ENST00000377075.2:c.468_482delinsCGACGGGCCCTGGCT	ENSP00000366275.2:p.Pro156=
NM_020184.3:c.468_482delinsCGACGGGCCCTGGCT	NP_064569.3:p.Pro156=
XM_005263914.2:c.468_482delinsCGACGGGCCCTGGCT	XP_005263971.1:p.Pro156=
XM_005263915.2:c.468_482delinsCGACGGGCCCTGGCT	XP_005263972.1:p.Pro156=
XM_011510955.1:c.468_482delinsCGACGGGCCCTGGCT	XP_011509257.1:p.Pro156=
XM_011510956.1:c.468_482delinsCGACGGGCCCTGGCT	XP_011509258.1:p.Pro156=
XM_005263914.4:c.468_482delinsCGACGGGCCCTGGCT	XP_005263971.1:p.Pro156=
XM_005263915.4:c.468_482delinsCGACGGGCCCTGGCT	XP_005263972.1:p.Pro156=
XM_011510955.3:c.468_482delinsCGACGGGCCCTGGCT	XP_011509257.1:p.Pro156=
XM_011510956.3:c.468_482delinsCGACGGGCCCTGGCT	XP_011509258.1:p.Pro156=
NM_020184.4:c.468_482delinsCGACGGGCCCTGGCT MANE Select	NP_064569.3:p.Pro156=