Canonical Allele Identifier: CA2674441307

Gene: MSH3 DHFR

Linked Data

• gnomAD v4: 5-80654910-A-AGCGCCCGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654916_80654917insGCGGCGCCC , CM000667.2:g.80654916_80654917insGCGGCGCCC	GRCh38
NC_000005.9:g.79950735_79950736insGCGGCGCCC , CM000667.1:g.79950735_79950736insGCGGCGCCC	GRCh37
NC_000005.8:g.79986491_79986492insGCGGCGCCC	NCBI36
NG_016607.1:g.5442_5443insGCGGCGCCC
NG_023304.1:g.5071_5072insCGCGGGCGC
NG_016607.2:g.5442_5443insGCGGCGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.189_190insGCGGCGCCC (MSH3) MANE Select	ENSP00000265081.6:p.Pro63_Pro64insAlaAlaPro
ENST00000439211.7:c.-422_-421insCGCGGGCGC (DHFR) MANE Select	ENSP00000396308.2:n.-422_-421insCGCGGGCGC
ENST00000667069.1:c.189_190insGCGGCGCCC (MSH3)	ENSP00000499502.1:p.Pro63_Pro64insAlaAlaPro
ENST00000670357.1:c.189_190insGCGGCGCCC (MSH3)	ENSP00000499791.1:p.Pro63_Pro64insAlaAlaPro
ENST00000265081.6:c.189_190insGCGGCGCCC (MSH3)	ENSP00000265081.6:p.Pro63_Pro64insAlaAlaPro
ENST00000439211.6:c.-422_-421insCGCGGGCGC (DHFR)	ENSP00000396308.2:n.-422_-421insCGCGGGCGC
NM_000791.3:c.-422_-421insCGCGGGCGC (DHFR)	NP_000782.1:n.-422_-421insCGCGGGCGC
NM_001290354.1:c.-528_-527insCGCGGGCGC (DHFR)	NP_001277283.1:n.-528_-527insCGCGGGCGC
NM_001290357.1:c.-422_-421insCGCGGGCGC (DHFR)	NP_001277286.1:n.-422_-421insCGCGGGCGC
NM_002439.4:c.189_190insGCGGCGCCC (MSH3)	NP_002430.3:p.Pro63_Pro64insAlaAlaPro
NR_110936.1:n.71_72insCGCGGGCGC (DHFR)
NM_000791.4:c.-422_-421insCGCGGGCGC (DHFR) MANE Select	NP_000782.1:n.-422_-421insCGCGGGCGC
NM_002439.5:c.189_190insGCGGCGCCC (MSH3) MANE Select	NP_002430.3:p.Pro63_Pro64insAlaAlaPro
NM_001290354.2:c.-528_-527insCGCGGGCGC (DHFR)	NP_001277283.1:n.-528_-527insCGCGGGCGC
NM_001290357.2:c.-422_-421insCGCGGGCGC (DHFR)	NP_001277286.1:n.-422_-421insCGCGGGCGC
NR_110936.2:n.73_74insCGCGGGCGC (DHFR)