Canonical Allele Identifier: CA1573632253

Gene: MCC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113063597_113063599delinsCAG , CM000667.2:g.113063597_113063599delinsCAG	GRCh38
NC_000005.9:g.112399294_112399296delinsCAG , CM000667.1:g.112399294_112399296delinsCAG	GRCh37
NC_000005.8:g.112427193_112427195delinsCAG	NCBI36
NG_012265.1:g.430232_430234delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302475.9:c.1643+385_1643+387delinsCTG	ENSP00000305617.4:n.1643+385_1643+387delinsCTG
ENST00000408903.7:c.2213+385_2213+387delinsCTG MANE Select	ENSP00000386227.3:n.2213+385_2213+387delinsCTG
ENST00000302475.8:c.1643+385_1643+387delinsCTG	ENSP00000305617.4:n.1643+385_1643+387delinsCTG
ENST00000408903.6:c.2213+385_2213+387delinsCTG	ENSP00000386227.3:n.2213+385_2213+387delinsCTG
ENST00000514701.5:c.1643+385_1643+387delinsCTG	ENSP00000485220.1:n.1643+385_1643+387delinsCTG
ENST00000515367.6:c.1454+385_1454+387delinsCTG	ENSP00000421615.2:n.1454+385_1454+387delinsCTG
ENST00000624689.3:c.57+385_57+387delinsCTG
NM_001085377.1:c.2213+385_2213+387delinsCTG	NP_001078846.1:n.2213+385_2213+387delinsCTG
NM_002387.2:c.1643+385_1643+387delinsCTG	NP_002378.1:n.1643+385_1643+387delinsCTG
XM_005271991.2:c.1643+385_1643+387delinsCTG	XP_005272048.1:n.1643+385_1643+387delinsCTG
XM_005271991.3:c.1643+385_1643+387delinsCTG	XP_005272048.1:n.1643+385_1643+387delinsCTG
XM_017009473.1:c.2213+385_2213+387delinsCTG	XP_016864962.1:n.2213+385_2213+387delinsCTG
XM_017009474.1:c.1613+385_1613+387delinsCTG	XP_016864963.1:n.1613+385_1613+387delinsCTG
XM_024446049.1:c.1454+385_1454+387delinsCTG	XP_024301817.1:n.1454+385_1454+387delinsCTG
XM_024446050.1:c.1454+385_1454+387delinsCTG	XP_024301818.1:n.1454+385_1454+387delinsCTG
XM_024446051.1:c.1454+385_1454+387delinsCTG	XP_024301819.1:n.1454+385_1454+387delinsCTG
XM_024446052.1:c.1454+385_1454+387delinsCTG	XP_024301820.1:n.1454+385_1454+387delinsCTG
NM_001085377.2:c.2213+385_2213+387delinsCTG MANE Select	NP_001078846.2:n.2213+385_2213+387delinsCTG
NM_002387.3:c.1643+385_1643+387delinsCTG	NP_002378.2:n.1643+385_1643+387delinsCTG