Canonical Allele Identifier: CA2573140040

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654710_80654754del , CM000667.2:g.80654710_80654754del	GRCh38
NC_000005.9:g.79950529_79950573del , CM000667.1:g.79950529_79950573del	GRCh37
NC_000005.8:g.79986285_79986329del	NCBI36
NG_016607.1:g.5236_5280del
NG_023304.1:g.5233_5277del
NG_016607.2:g.5236_5280del

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-260_-216del (DHFR) MANE Select	NP_000782.1:n.-260_-216del
ENST00000439211.7:c.-260_-216del (DHFR) MANE Select	ENSP00000396308.2:n.-260_-216del
NM_000791.3:c.-260_-216del (DHFR)	NP_000782.1:n.-260_-216del
NM_001290354.1:c.-366_-322del (DHFR)	NP_001277283.1:n.-366_-322del
NM_001290354.2:c.-366_-322del (DHFR)	NP_001277283.1:n.-366_-322del
NM_001290357.1:c.-260_-216del (DHFR)	NP_001277286.1:n.-260_-216del
NM_001290357.2:c.-260_-216del (DHFR)	NP_001277286.1:n.-260_-216del
NM_002439.4:c.-18_27del (MSH3)
NM_002439.5:c.-18_27del (MSH3)
NR_110936.1:n.233_277del (DHFR)
NR_110936.2:n.235_279del (DHFR)
ENST00000265081.6:c.-18_27del (MSH3)
ENST00000265081.7:c.-18_27del (MSH3)
ENST00000439211.6:c.-260_-216del (DHFR)	ENSP00000396308.2:n.-260_-216del
ENST00000667069.1:c.-18_27del (MSH3)
ENST00000670357.1:c.-18_27del (MSH3)