Canonical Allele Identifier: CA1272753215

Gene: CNNM4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96761618_96761620delinsATG , CM000664.2:g.96761618_96761620delinsATG	GRCh38
NC_000002.11:g.97427355_97427357delinsATG , CM000664.1:g.97427355_97427357delinsATG	GRCh37
NC_000002.10:g.96791082_96791084delinsATG	NCBI36
NG_016608.1:g.5717_5719delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.619_621delinsATG MANE Select	ENSP00000366275.2:p.Met207=
ENST00000377075.2:c.619_621delinsATG	ENSP00000366275.2:p.Met207=
NM_020184.3:c.619_621delinsATG	NP_064569.3:p.Met207=
XM_005263914.2:c.619_621delinsATG	XP_005263971.1:p.Met207=
XM_005263915.2:c.619_621delinsATG	XP_005263972.1:p.Met207=
XM_011510955.1:c.619_621delinsATG	XP_011509257.1:p.Met207=
XM_011510956.1:c.619_621delinsATG	XP_011509258.1:p.Met207=
XM_005263914.4:c.619_621delinsATG	XP_005263971.1:p.Met207=
XM_005263915.4:c.619_621delinsATG	XP_005263972.1:p.Met207=
XM_011510955.3:c.619_621delinsATG	XP_011509257.1:p.Met207=
XM_011510956.3:c.619_621delinsATG	XP_011509258.1:p.Met207=
NM_020184.4:c.619_621delinsATG MANE Select	NP_064569.3:p.Met207=