Canonical Allele Identifier: CA2580073510

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654798del , CM000667.2:g.80654798del	GRCh38
NC_000005.9:g.79950617del , CM000667.1:g.79950617del	GRCh37
NC_000005.8:g.79986373del	NCBI36
NG_016607.1:g.5324del
NG_023304.1:g.5187del
NG_016607.2:g.5324del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.71del (MSH3) MANE Select	ENSP00000265081.6:p.Leu24Ter
ENST00000439211.7:c.-306del (DHFR) MANE Select	ENSP00000396308.2:n.-306del
ENST00000667069.1:c.71del (MSH3)	ENSP00000499502.1:p.Leu24Ter
ENST00000670357.1:c.71del (MSH3)	ENSP00000499791.1:p.Leu24Ter
ENST00000265081.6:c.71del (MSH3)	ENSP00000265081.6:p.Leu24Ter
ENST00000439211.6:c.-306del (DHFR)	ENSP00000396308.2:n.-306del
NM_000791.3:c.-306del (DHFR)	NP_000782.1:n.-306del
NM_001290354.1:c.-412del (DHFR)	NP_001277283.1:n.-412del
NM_001290357.1:c.-306del (DHFR)	NP_001277286.1:n.-306del
NM_002439.4:c.71del (MSH3)	NP_002430.3:p.Leu24Ter
NR_110936.1:n.187del (DHFR)
NM_000791.4:c.-306del (DHFR) MANE Select	NP_000782.1:n.-306del
NM_002439.5:c.71del (MSH3) MANE Select	NP_002430.3:p.Leu24Ter
NM_001290354.2:c.-412del (DHFR)	NP_001277283.1:n.-412del
NM_001290357.2:c.-306del (DHFR)	NP_001277286.1:n.-306del
NR_110936.2:n.189del (DHFR)