Canonical Allele Identifier: CA3273060

Gene: MAP3K1

Linked Data

• dbSNP Id: rs768585757
• ExAC: 5:56177838 A / AAATCAAACAATTGGCAAGAACTTCTTGGCCG
• MyVariant Identifiers: chr5:g.56177838_56177839insAATCAAACAATTGGCAAGAACTTCTTGGCCG (hg19) ; chr5:g.56882011_56882012insAATCAAACAATTGGCAAGAACTTCTTGGCCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882011_56882012insAATCAAACAATTGGCAAGAACTTCTTGGCCG , CM000667.2:g.56882011_56882012insAATCAAACAATTGGCAAGAACTTCTTGGCCG	GRCh38
NC_000005.9:g.56177838_56177839insAATCAAACAATTGGCAAGAACTTCTTGGCCG , CM000667.1:g.56177838_56177839insAATCAAACAATTGGCAAGAACTTCTTGGCCG	GRCh37
NC_000005.8:g.56213595_56213596insAATCAAACAATTGGCAAGAACTTCTTGGCCG	NCBI36
NG_031884.1:g.71939_71940insAATCAAACAATTGGCAAGAACTTCTTGGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2811_2812insAATCAAACAATTGGCAAGAACTTCTTGGCCG MANE Select	ENSP00000382423.3:p.Pro938AsnfsTer13
ENST00000399503.3:c.2811_2812insAATCAAACAATTGGCAAGAACTTCTTGGCCG	ENSP00000382423.3:p.Pro938AsnfsTer13
NM_005921.1:c.2811_2812insAATCAAACAATTGGCAAGAACTTCTTGGCCG	NP_005912.1:p.Pro938AsnfsTer13
XM_005248519.3:c.2433_2434insAATCAAACAATTGGCAAGAACTTCTTGGCCG	XP_005248576.2:p.Pro812AsnfsTer13
XM_011543406.1:c.2556_2557insAATCAAACAATTGGCAAGAACTTCTTGGCCG	XP_011541708.1:p.Pro853AsnfsTer13
XM_011543407.1:c.2532_2533insAATCAAACAATTGGCAAGAACTTCTTGGCCG	XP_011541709.1:p.Pro845AsnfsTer13
XM_011543408.1:c.2811_2812insAATCAAACAATTGGCAAGAACTTCTTGGCCG	XP_011541710.1:p.Pro938AsnfsTer13
XM_017009484.1:c.2400_2401insAATCAAACAATTGGCAAGAACTTCTTGGCCG	XP_016864973.1:p.Pro801AsnfsTer13
XM_017009485.1:c.2322_2323insAATCAAACAATTGGCAAGAACTTCTTGGCCG	XP_016864974.1:p.Pro775AsnfsTer13
XR_001742068.2:n.2842_2843insAATCAAACAATTGGCAAGAACTTCTTGGCCG
NM_005921.2:c.2811_2812insAATCAAACAATTGGCAAGAACTTCTTGGCCG MANE Select	NP_005912.1:p.Pro938AsnfsTer13