Canonical Allele Identifier: CA1425384275

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183042145_183042146delinsAG , CM000665.2:g.183042145_183042146delinsAG	GRCh38
NC_000003.11:g.182759933_182759934delinsAG , CM000665.1:g.182759933_182759934delinsAG	GRCh37
NC_000003.10:g.184242627_184242628delinsAG	NCBI36
NG_008100.1:g.62432_62433delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1084-396_1084-395delinsCT MANE Select	ENSP00000265594.4:n.1084-396_1084-395delinsCT
ENST00000265594.8:c.1084-396_1084-395delinsCT	ENSP00000265594.4:n.1084-396_1084-395delinsCT
ENST00000476176.5:c.943-396_943-395delinsCT	ENSP00000420433.1:n.943-396_943-395delinsCT
ENST00000492597.5:c.757-396_757-395delinsCT	ENSP00000419898.1:n.757-396_757-395delinsCT
ENST00000495767.5:c.*665-396_*665-395delinsCT	ENSP00000419658.1:n.*665-396_*665-395delinsCT
ENST00000497830.5:c.*681-396_*681-395delinsCT	ENSP00000420088.1:n.*681-396_*681-395delinsCT
ENST00000497959.5:c.970-396_970-395delinsCT	ENSP00000420648.1:n.970-396_970-395delinsCT
ENST00000539926.5:c.634-396_634-395delinsCT	ENSP00000441253.2:n.634-396_634-395delinsCT
ENST00000610757.4:c.634-396_634-395delinsCT	ENSP00000480435.1:n.634-396_634-395delinsCT
ENST00000629669.2:c.970-396_970-395delinsCT	ENSP00000486824.1:n.970-396_970-395delinsCT
NM_001293273.1:c.733-396_733-395delinsCT	NP_001280202.1:n.733-396_733-395delinsCT
NM_020166.4:c.1084-396_1084-395delinsCT	NP_064551.3:n.1084-396_1084-395delinsCT
NR_120639.1:n.998-396_998-395delinsCT
NR_120640.1:n.1751-396_1751-395delinsCT
XM_006713702.1:c.757-396_757-395delinsCT	XP_006713765.1:n.757-396_757-395delinsCT
XM_011512992.1:c.970-396_970-395delinsCT	XP_011511294.1:n.970-396_970-395delinsCT
XM_011512993.1:c.1084-396_1084-395delinsCT	XP_011511295.1:n.1084-396_1084-395delinsCT
XR_241502.2:n.1231-396_1231-395delinsCT
XR_924159.1:n.1231-396_1231-395delinsCT
NM_001363880.1:c.757-396_757-395delinsCT	NP_001350809.1:n.757-396_757-395delinsCT
XM_011512992.2:c.970-396_970-395delinsCT	XP_011511294.1:n.970-396_970-395delinsCT
XR_001740207.2:n.1207-396_1207-395delinsCT
XR_001740208.2:n.1207-396_1207-395delinsCT
XR_001740209.2:n.1177-396_1177-395delinsCT
XR_001740210.1:n.1037-396_1037-395delinsCT
XR_002959553.1:n.1207-396_1207-395delinsCT
XR_002959554.1:n.1207-396_1207-395delinsCT
XR_241502.3:n.1177-396_1177-395delinsCT
NM_020166.5:c.1084-396_1084-395delinsCT MANE Select	NP_064551.3:n.1084-396_1084-395delinsCT
NM_001293273.2:c.733-396_733-395delinsCT	NP_001280202.1:n.733-396_733-395delinsCT
NR_120639.2:n.907-396_907-395delinsCT
NR_120640.2:n.1751-396_1751-395delinsCT