Canonical Allele Identifier: CA2709118299

Gene: MSH3 DHFR

Linked Data

• dbSNP Id: rs1749214765

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654916_80654917insGCAGCGCCG , CM000667.2:g.80654916_80654917insGCAGCGCCG	GRCh38
NC_000005.9:g.79950735_79950736insGCAGCGCCG , CM000667.1:g.79950735_79950736insGCAGCGCCG	GRCh37
NC_000005.8:g.79986491_79986492insGCAGCGCCG	NCBI36
NG_016607.1:g.5442_5443insGCAGCGCCG
NG_023304.1:g.5065_5066insCGGCGCTGC
NG_016607.2:g.5442_5443insGCAGCGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.189_190insGCAGCGCCG (MSH3) MANE Select	ENSP00000265081.6:p.Pro63_Pro64insAlaAlaPro
ENST00000439211.7:c.-428_-427insCGGCGCTGC (DHFR) MANE Select	ENSP00000396308.2:n.-428_-427insCGGCGCTGC
ENST00000667069.1:c.189_190insGCAGCGCCG (MSH3)	ENSP00000499502.1:p.Pro63_Pro64insAlaAlaPro
ENST00000670357.1:c.189_190insGCAGCGCCG (MSH3)	ENSP00000499791.1:p.Pro63_Pro64insAlaAlaPro
ENST00000265081.6:c.189_190insGCAGCGCCG (MSH3)	ENSP00000265081.6:p.Pro63_Pro64insAlaAlaPro
ENST00000439211.6:c.-428_-427insCGGCGCTGC (DHFR)	ENSP00000396308.2:n.-428_-427insCGGCGCTGC
NM_000791.3:c.-428_-427insCGGCGCTGC (DHFR)	NP_000782.1:n.-428_-427insCGGCGCTGC
NM_001290354.1:c.-534_-533insCGGCGCTGC (DHFR)	NP_001277283.1:n.-534_-533insCGGCGCTGC
NM_001290357.1:c.-428_-427insCGGCGCTGC (DHFR)	NP_001277286.1:n.-428_-427insCGGCGCTGC
NM_002439.4:c.189_190insGCAGCGCCG (MSH3)	NP_002430.3:p.Pro63_Pro64insAlaAlaPro
NR_110936.1:n.65_66insCGGCGCTGC (DHFR)
NM_000791.4:c.-428_-427insCGGCGCTGC (DHFR) MANE Select	NP_000782.1:n.-428_-427insCGGCGCTGC
NM_002439.5:c.189_190insGCAGCGCCG (MSH3) MANE Select	NP_002430.3:p.Pro63_Pro64insAlaAlaPro
NM_001290354.2:c.-534_-533insCGGCGCTGC (DHFR)	NP_001277283.1:n.-534_-533insCGGCGCTGC
NM_001290357.2:c.-428_-427insCGGCGCTGC (DHFR)	NP_001277286.1:n.-428_-427insCGGCGCTGC
NR_110936.2:n.67_68insCGGCGCTGC (DHFR)