Canonical Allele Identifier: CA2674441052

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654867_80654899del , CM000667.2:g.80654867_80654899del	GRCh38
NC_000005.9:g.79950686_79950718del , CM000667.1:g.79950686_79950718del	GRCh37
NC_000005.8:g.79986442_79986474del	NCBI36
NG_016607.1:g.5393_5425del
NG_023304.1:g.5084_5116del
NG_016607.2:g.5393_5425del

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-409_-377del (DHFR) MANE Select	NP_000782.1:n.-409_-377del
NM_002439.5:c.140_172del (MSH3) MANE Select	NP_002430.3:p.Val47_Ala57del
ENST00000265081.7:c.140_172del (MSH3) MANE Select	ENSP00000265081.6:p.Val47_Ala57del
ENST00000439211.7:c.-409_-377del (DHFR) MANE Select	ENSP00000396308.2:n.-409_-377del
NM_000791.3:c.-409_-377del (DHFR)	NP_000782.1:n.-409_-377del
NM_001290354.1:c.-515_-483del (DHFR)	NP_001277283.1:n.-515_-483del
NM_001290354.2:c.-515_-483del (DHFR)	NP_001277283.1:n.-515_-483del
NM_001290357.1:c.-409_-377del (DHFR)	NP_001277286.1:n.-409_-377del
NM_001290357.2:c.-409_-377del (DHFR)	NP_001277286.1:n.-409_-377del
NM_002439.4:c.140_172del (MSH3)	NP_002430.3:p.Val47_Ala57del
NR_110936.1:n.84_116del (DHFR)
NR_110936.2:n.86_118del (DHFR)
ENST00000265081.6:c.140_172del (MSH3)	ENSP00000265081.6:p.Val47_Ala57del
ENST00000439211.6:c.-409_-377del (DHFR)	ENSP00000396308.2:n.-409_-377del
ENST00000667069.1:c.140_172del (MSH3)	ENSP00000499502.1:p.Val47_Ala57del
ENST00000670357.1:c.140_172del (MSH3)	ENSP00000499791.1:p.Val47_Ala57del