Canonical Allele Identifier: CA2674441218

Gene: MSH3 DHFR

Linked Data

• gnomAD v4: 5-80654907-C-CGCAGCGCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654915_80654916insAGCAGCGCC , CM000667.2:g.80654915_80654916insAGCAGCGCC	GRCh38
NC_000005.9:g.79950734_79950735insAGCAGCGCC , CM000667.1:g.79950734_79950735insAGCAGCGCC	GRCh37
NC_000005.8:g.79986490_79986491insAGCAGCGCC	NCBI36
NG_016607.1:g.5441_5442insAGCAGCGCC
NG_023304.1:g.5074_5075insTGGCGCTGC
NG_016607.2:g.5441_5442insAGCAGCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.188_189insAGCAGCGCC (MSH3) MANE Select	ENSP00000265081.6:p.Pro63_Pro64insAlaAlaPro
ENST00000439211.7:c.-419_-418insTGGCGCTGC (DHFR) MANE Select	ENSP00000396308.2:n.-419_-418insTGGCGCTGC
ENST00000667069.1:c.188_189insAGCAGCGCC (MSH3)	ENSP00000499502.1:p.Pro63_Pro64insAlaAlaPro
ENST00000670357.1:c.188_189insAGCAGCGCC (MSH3)	ENSP00000499791.1:p.Pro63_Pro64insAlaAlaPro
ENST00000265081.6:c.188_189insAGCAGCGCC (MSH3)	ENSP00000265081.6:p.Pro63_Pro64insAlaAlaPro
ENST00000439211.6:c.-419_-418insTGGCGCTGC (DHFR)	ENSP00000396308.2:n.-419_-418insTGGCGCTGC
NM_000791.3:c.-419_-418insTGGCGCTGC (DHFR)	NP_000782.1:n.-419_-418insTGGCGCTGC
NM_001290354.1:c.-525_-524insTGGCGCTGC (DHFR)	NP_001277283.1:n.-525_-524insTGGCGCTGC
NM_001290357.1:c.-419_-418insTGGCGCTGC (DHFR)	NP_001277286.1:n.-419_-418insTGGCGCTGC
NM_002439.4:c.188_189insAGCAGCGCC (MSH3)	NP_002430.3:p.Pro63_Pro64insAlaAlaPro
NR_110936.1:n.74_75insTGGCGCTGC (DHFR)
NM_000791.4:c.-419_-418insTGGCGCTGC (DHFR) MANE Select	NP_000782.1:n.-419_-418insTGGCGCTGC
NM_002439.5:c.188_189insAGCAGCGCC (MSH3) MANE Select	NP_002430.3:p.Pro63_Pro64insAlaAlaPro
NM_001290354.2:c.-525_-524insTGGCGCTGC (DHFR)	NP_001277283.1:n.-525_-524insTGGCGCTGC
NM_001290357.2:c.-419_-418insTGGCGCTGC (DHFR)	NP_001277286.1:n.-419_-418insTGGCGCTGC
NR_110936.2:n.76_77insTGGCGCTGC (DHFR)