Canonical Allele Identifier: CA1573632485

Gene: MCC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113063995_113063997delinsGTT , CM000667.2:g.113063995_113063997delinsGTT	GRCh38
NC_000005.9:g.112399692_112399694delinsGTT , CM000667.1:g.112399692_112399694delinsGTT	GRCh37
NC_000005.8:g.112427591_112427593delinsGTT	NCBI36
NG_012265.1:g.429834_429836delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302475.9:c.1630_1632delinsAAC	ENSP00000305617.4:p.Asn544=
ENST00000408903.7:c.2200_2202delinsAAC MANE Select	ENSP00000386227.3:p.Asn734=
ENST00000302475.8:c.1630_1632delinsAAC	ENSP00000305617.4:p.Asn544=
ENST00000408903.6:c.2200_2202delinsAAC	ENSP00000386227.3:p.Asn734=
ENST00000514701.5:c.1630_1632delinsAAC	ENSP00000485220.1:p.Asn544=
ENST00000515367.6:c.1441_1443delinsAAC	ENSP00000421615.2:p.Asn481=
ENST00000624689.3:c.44_46delinsAAC
NM_001085377.1:c.2200_2202delinsAAC	NP_001078846.1:p.Asn734=
NM_002387.2:c.1630_1632delinsAAC	NP_002378.1:p.Asn544=
XM_005271991.2:c.1630_1632delinsAAC	XP_005272048.1:p.Asn544=
XM_005271991.3:c.1630_1632delinsAAC	XP_005272048.1:p.Asn544=
XM_017009473.1:c.2200_2202delinsAAC	XP_016864962.1:p.Asn734=
XM_017009474.1:c.1600_1602delinsAAC	XP_016864963.1:p.Asn534=
XM_024446049.1:c.1441_1443delinsAAC	XP_024301817.1:p.Asn481=
XM_024446050.1:c.1441_1443delinsAAC	XP_024301818.1:p.Asn481=
XM_024446051.1:c.1441_1443delinsAAC	XP_024301819.1:p.Asn481=
XM_024446052.1:c.1441_1443delinsAAC	XP_024301820.1:p.Asn481=
NM_001085377.2:c.2200_2202delinsAAC MANE Select	NP_001078846.2:p.Asn734=
NM_002387.3:c.1630_1632delinsAAC	NP_002378.2:p.Asn544=