Canonical Allele Identifier: CA2674882399

Gene: MCC

Linked Data

• gnomAD v4: 5-113064043-AAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113064044_113064046del , CM000667.2:g.113064044_113064046del	GRCh38
NC_000005.9:g.112399741_112399743del , CM000667.1:g.112399741_112399743del	GRCh37
NC_000005.8:g.112427640_112427642del	NCBI36
NG_012265.1:g.429785_429787del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302475.9:c.1581_1583del	ENSP00000305617.4:p.Phe528del
ENST00000408903.7:c.2151_2153del MANE Select	ENSP00000386227.3:p.Phe718del
ENST00000302475.8:c.1581_1583del	ENSP00000305617.4:p.Phe528del
ENST00000408903.6:c.2151_2153del	ENSP00000386227.3:p.Phe718del
ENST00000514701.5:c.1581_1583del	ENSP00000485220.1:p.Phe528del
ENST00000515367.6:c.1392_1394del	ENSP00000421615.2:p.Phe465del
NM_001085377.1:c.2151_2153del	NP_001078846.1:p.Phe718del
NM_002387.2:c.1581_1583del	NP_002378.1:p.Phe528del
XM_005271991.2:c.1581_1583del	XP_005272048.1:p.Phe528del
XM_005271991.3:c.1581_1583del	XP_005272048.1:p.Phe528del
XM_017009473.1:c.2151_2153del	XP_016864962.1:p.Phe718del
XM_017009474.1:c.1551_1553del	XP_016864963.1:p.Phe518del
XM_024446049.1:c.1392_1394del	XP_024301817.1:p.Phe465del
XM_024446050.1:c.1392_1394del	XP_024301818.1:p.Phe465del
XM_024446051.1:c.1392_1394del	XP_024301819.1:p.Phe465del
XM_024446052.1:c.1392_1394del	XP_024301820.1:p.Phe465del
NM_001085377.2:c.2151_2153del MANE Select	NP_001078846.2:p.Phe718del
NM_002387.3:c.1581_1583del	NP_002378.2:p.Phe528del