Canonical Allele Identifier: CA2693084113

Gene: MID1

Linked Data

• gnomAD v4: X-10459611-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.10459611A>G , CM000685.2:g.10459611A>G	GRCh38
NC_000023.10:g.10427651A>G , CM000685.1:g.10427651A>G	GRCh37
NC_000023.9:g.10387651A>G	NCBI36
NG_008197.1:g.379080T>C
NG_008197.2:g.379080T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413894.6:c.1447+35T>C	ENSP00000391154.2:n.1447+35T>C
ENST00000689773.1:c.1333+35T>C	ENSP00000509925.1:n.1333+35T>C
ENST00000690004.1:c.1333+35T>C	ENSP00000509730.1:n.1333+35T>C
ENST00000691943.1:c.1339+35T>C	ENSP00000508663.1:n.1339+35T>C
ENST00000317552.9:c.1447+35T>C MANE Select	ENSP00000312678.4:n.1447+35T>C
ENST00000674917.1:c.580+35T>C	ENSP00000502171.1:n.580+35T>C
ENST00000675073.1:c.1600+35T>C	ENSP00000501707.1:n.1600+35T>C
ENST00000317552.8:c.1447+35T>C	ENSP00000312678.4:n.1447+35T>C
ENST00000380779.5:c.1447+35T>C	ENSP00000370156.1:n.1447+35T>C
ENST00000380780.5:c.1447+35T>C	ENSP00000370157.1:n.1447+35T>C
ENST00000380782.6:c.1447+35T>C	ENSP00000370159.1:n.1447+35T>C
ENST00000380785.5:c.1447+35T>C	ENSP00000370162.1:n.1447+35T>C
ENST00000380787.5:c.1447+35T>C	ENSP00000370164.1:n.1447+35T>C
ENST00000413894.5:c.1447+35T>C	ENSP00000391154.1:n.1447+35T>C
ENST00000453318.6:c.1447+35T>C	ENSP00000414521.2:n.1447+35T>C
ENST00000479925.1:n.397+35T>C
NM_000381.3:c.1447+35T>C	NP_000372.1:n.1447+35T>C
NM_001098624.2:c.1447+35T>C	NP_001092094.1:n.1447+35T>C
NM_001193277.1:c.1447+35T>C	NP_001180206.1:n.1447+35T>C
NM_033289.1:c.1333+35T>C	NP_150631.1:n.1333+35T>C
NM_033290.3:c.1447+35T>C	NP_150632.1:n.1447+35T>C
XM_005274536.1:c.1600+35T>C	XP_005274593.1:n.1600+35T>C
XM_005274537.1:c.1600+35T>C	XP_005274594.1:n.1600+35T>C
XM_006724492.2:c.1600+35T>C	XP_006724555.1:n.1600+35T>C
XM_006724493.2:c.1486+35T>C	XP_006724556.1:n.1486+35T>C
XM_011545525.1:c.1600+35T>C	XP_011543827.1:n.1600+35T>C
XM_011545526.1:c.1600+35T>C	XP_011543828.1:n.1600+35T>C
XM_011545527.1:c.1600+35T>C	XP_011543829.1:n.1600+35T>C
NM_001347733.1:c.1447+35T>C	NP_001334662.1:n.1447+35T>C
NM_000381.4:c.1447+35T>C MANE Select	NP_000372.1:n.1447+35T>C
NM_001347733.2:c.1447+35T>C	NP_001334662.1:n.1447+35T>C
NM_033289.2:c.1333+35T>C	NP_150631.1:n.1333+35T>C
NM_033290.4:c.1447+35T>C	NP_150632.1:n.1447+35T>C